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Autism is a syndrome characterized by impairments in social relatedness,
language and communication, a need for routine and sameness, abnormal
movements, and sensory dysfunction. Mercury (Hg) is a toxic metal that can
exist as a pure element or in a variety of inorganic and organic forms and can
cause immune, sensory, neurological, motor, and behavioral dysfunctions similar
to traits defining or associated with autism. Thimerosal, a preservative
frequently added to childhood vaccines, has become a major source of Hg in
human infants and toddlers. According to the FDA and the American Academy of
Pediatricians, fully vaccinated children now receive, within their first two
years, Hg levels that exceed safety limits established by the FDA and other
supervisory agencies. A thorough review of medical literature and U.S.
government data indicates (i) that many and perhaps most cases of idiopathic
autism, in which an extended period of developmental normalcy is followed by an
emergence of symptoms, are induced by early exposure to Hg; (ii) that this type
of autism represents a unique form of Hg poisoning (HgP); (iii) that excessive
Hg exposure from thimerosal in vaccine injections is an etiological mechanism
for causing the traits of autism; (iv) that certain genetic and non-genetic
factors establish a predisposition whereby thimerosal's adverse effects occur
only in some children; and (v) that vaccinal Hg in thimerosal is causing a
heretofore unrecognized mercurial syndrome.
A review of medical literature indicates that the characteristics of autism
and of mercury poisoning (HgP) are strikingly similar. Traits defining or
associated with both disorders are summarized in Table A immediately following
the Table of Contents and are discussed and cited in the body of this
document. The parallels between the two diseases are so thorough as to suggest,
based on total Hg injected into U.S. children, that many cases of autism are a
form of mercury poisoning.
For these children, the exposure route is childhood vaccines, most of which
contain thimerosal, a preservative which is 49.6% ethylmercury by weight. The
amount of mercury a typical child under two years receives from vaccinations
equates to 237.5 micrograms, or 3.53 x 1017 molecules (353,000,000,000,000,000
molecules). Most such vaccinal Hg may not be excreted and instead migrates to
the brain.
The total amount injected into infants and toddlers (i) is known to exceed
Federal safety standards, (ii) is officially considered to be a “low” level;
whereby (iii) only a small percentage of exposed individuals exhibit symptoms
of toxicity. In fact, children who develop Hg-related autism are likely to have
had a predisposition derived from genetic and non-genetic factors.
Importantly, the timings of vaccinal Hg-exposure and its latency period
coincide with the emergence of autistic-symptoms in specific children.
Moreover, excessive mercury has been detected in urine, hair, and blood samples
from autistic children; and parental reports, though limited at this date,
indicate significant improvement in symptoms subsequent to heavy-metal
chelation therapy.
The HgP phenotype is diverse and depends upon a number of factors -
including type of Hg, route of entry into the body, rate and level of dose,
individual genotype, and the age and immune status of the patient.
Historically, variation among these factors has caused slightly different
manifestations of mercurialism; Mad Hatter’s disease, Minamata disease,
acrodynia, and industrial exposures provide examples.
The pathology arising from the mercury-related variables involved in autism
- intermittent bolus doses of ethylmercury injected into susceptible infants
and toddlers - is heretofore undescribed in medical literature. Therefore, in
accord with existing HgP data and HgP’s ability to induce virtually all the
traits defining or associated with autism spectrum disorders, we hypothesize that
many and perhaps most cases of autism represent a unique form of mercury
poisoning.
This conclusion and its supporting data have important implications for the
affected population of autistic individuals and their families, for other
unexplained disorders with symptoms similar to those of heavy metal
intoxication, for vaccine content, and for childhood vaccination programs. Due
to its high potential for neurotoxicity, thimerosal should be removed
immediately from all vaccine products designated for infants and toddlers.
ABSTRACT & SYNOPSIS
TABLE OF CONTENTS
AUTISM-MERCURIALISM COMPARISONS
INTRODUCTION
Autism
Mercury
Diagnosing Mercury Poisoning in Autism
I. SYMPTOM COMPARISON
a. Affect/Psychological Presentation
b. Language & Hearing
c. Sensory Perception
d. Movement/Motor Function
e. Cognition/Mental Function
f. Behaviors
g. Vision
h. Physical Presentations
j. Gastrointestinal Function
II. COMPARISON OF BIOLOGICAL ABNORMALITIES
a. Biochemistry
b. Immune System
c. CNS Structure
d. Neurons & Neurochemicals
e. EEG Activity/Epilepsy
III. MECHANISMS, SOURCES & EPIDEMIOLOGY OF EXPOSURE
a. Exposure Mechanism
b. Population Susceptibility
c. Sex Ratio
d. Exposure Levels & Autism
Prevalence
e. Genetic Factors
f. Course of Disease
g. Thimerosal Interaction with Vaccines
IV. DETECTION OF MERCURY IN AUTISTIC CHILDREN
Case Studies
Discussion
DISCUSSION
Diagnostic Criteria Are Met
Unique Form Would be Expected,
Implicates Vaccinal Thimerosal
Historical Precedent Exists
Barriers Preventing Earlier Discovery
Are Removed
MEDICAL & SOCIETAL IMPLICATIONS
Affected Population
Other Disorders
Vaccination Programs
|
Mercury
Poisoning |
Autism |
|
Psychiatric Disturbances |
|
|
Social deficits, shyness, social withdrawal |
Social deficits, social withdrawal, shyness |
|
Depression, mood swings; mask face |
Depressive traits, mood swings; flat affect |
|
Anxiety |
Anxiety |
|
Schizoid tendencies, OCD traits |
Schizophrenic & OCD traits; repetitiveness |
|
Lacks eye contact, hesitant to engage others |
Lack of eye contact, avoids conversation |
|
Irrational fears |
Irrational fears |
|
Irritability, aggression, temper tantrums |
Irritability, aggression, temper tantrums |
|
Impaired face recognition |
Impaired face recognition |
|
Speech, Language & Hearing Deficits |
|
|
Loss of speech, failure to develop speech |
Delayed language, failure to develop speech |
|
Dysarthria; articulation problems |
Dysarthria; articulation problems |
|
Speech comprehension deficits |
Speech comprehension deficits |
|
Verbalizing & word retrieval problems |
Echolalia; word use & pragmatic errors |
|
Sound sensitivity |
Sound sensitivity |
|
Hearing loss; deafness in very high doses |
Mild to profound hearing loss |
|
Poor performance on language IQ tests |
Poor performance on verbal IQ tests |
|
Sensory Abnormalities</TD< tr> |
|
|
Abnormal sensation in mouth & extremities |
Abnormal sensation in mouth & extremities |
|
Sound sensitivity |
Sound sensitivity |
|
Abnormal touch sensations; touch aversion |
Abnormal touch sensations; touch aversion |
|
Vestibular abnormalities |
Vestibular abnormalities |
|
Motor Disorders |
|
|
Involuntary jerking movements - arm flapping, ankle jerks,
myoclonal jerks, choreiform movements, circling, rocking |
Stereotyped movements - arm flapping, jumping, circling,
spinning, rocking; myoclonal jerks; choreiform movements |
|
Deficits in eye-hand coordination; limb apraxia; intention
tremors |
Poor eye-hand coordination; limb apraxia; problems with
intentional movements |
|
Gait impairment; ataxia - from incoordination &
clumsiness to inability to walk, stand, or sit; loss of motor control |
Abnormal gait and posture, clumsiness and incoordination;
difficulties sitting, lying, crawling, and walking |
|
Difficulty in chewing or swallowing |
Difficulty chewing or swallowing |
|
Unusual postures; toe walking |
Unusual postures; toe walking |
|
Cognitive Impairments |
|
|
Borderline intelligence, mental retardation - some cases
reversible |
Borderline intelligence, mental retardation - sometimes
"recovered" |
|
Poor concentration, attention, response inhibition |
Poor concentration, attention, shifting attention |
|
Uneven performance on IQ subtests |
Uneven performance on IQ subtests |
|
Verbal IQ higher than performance IQ |
Verbal IQ higher than performance IQ |
|
Poor short term, verbal, & auditory memory |
Poor short term, auditory & verbal memory |
|
Poor visual and perceptual motor skills, impairment in
simple reaction time |
Poor visual and perceptual motor skills, lower performance
on timed tests |
|
Difficulty carrying out complex commands |
Difficulty carrying out multiple commands |
|
Word-comprehension difficulties |
Word-comprehension difficulties |
|
Deficits in understanding abstract ideas & symbolism;
degeneration of higher mental powers |
Deficits in abstract thinking & symbolism,
understanding other’s mental states, sequencing, planning & organizing |
|
Unusual Behaviors |
|
|
Stereotyped sniffing (rats) |
Stereotyped, repetitive behaviors |
|
ADHD traits |
ADHD traits |
|
Agitation, unprovoked crying, grimacing, staring spells |
Agitation, unprovoked crying, grimacing, staring spells |
|
Sleep difficulties |
Sleep difficulties |
|
Eating disorders, feeding problems |
Eating disorders, feeding problems |
|
Self injurious behavior, e.g. head banging |
Self injurious behavior, e.g. head banging |
|
Visual Impairments |
|
|
Poor eye contact, impaired visual fixation |
Poor eye contact, problems in joint attention |
|
“Visual impairments,” blindness, near-sightedness,
decreased visual acuity |
“Visual impairments”; inaccurate/slow saccades; decreased
rod functioning |
|
Light sensitivity, photophobia |
Over-sensitivity to light |
|
Blurred or hazy vision |
Blurred vision |
|
Constricted visual fields |
Not described |
|
Physical Disturbances |
|
|
|
|
|
Increase in cerebral palsy; hyper- or hypo-tonia; abnormal
reflexes; decreased muscle strength, especially upper body; incontinence;
problems chewing, swallowing, salivating |
Increase in cerebral palsy; hyper- or hypotonia; decreased
muscle strength, especially upper body; incontinence; problems chewing and
swallowing |
|
Rashes, dermatitis/dry skin, itching; burning |
Rashes, dermatitis, eczema, itching |
|
Autonomic disturbance: excessive sweating, poor
circulation, elevated heart rate |
Autonomic disturbance: unusual sweating, poor circulation,
elevated heart rate |
|
Gastro-intestinal Disturbances</TD<
tr> |
|
|
Gastroenteritis, diarrhea; abdominal pain, constipation,
“colitis” |
Diarrhea, constipation, gaseousness, abdominal discomfort,
colitis |
|
Anorexia, weight loss, nausea, poor appetite |
Anorexia; feeding problems/vomiting |
|
Lesions of ileum & colon; increased gut permeability |
Leaky gut syndrome |
|
Inhibits dipeptidyl peptidase IV, which cleaves
casomorphin |
Inadequate endopeptidase enzymes needed for breakdown of
casein & gluten |
|
Abnormal Biochemistry |
|
|
Binds -SH groups; blocks sulfate transporter in
intestines, kidneys |
Low sulfate levels |
|
Has special affinity for purines & pyrimidines |
Purine & pyrimidine metabolism errors lead to autistic
features |
|
Reduces availability of glutathione, needed in neurons,
cells & liver to detoxify heavy metals |
Low levels of glutathione; decreased ability of liver to
detoxify heavy metals |
|
Causes significant reduction in glutathione peroxidase and
glutathione reductase |
Abnormal glutathione peroxidase activities in erythrocytes
|
|
Disrupts mitochondrial activities, especially in brain |
Mitochondrial dysfunction, especially in brain |
|
Immune Dysfunction |
|
|
Sensitivity due to allergic or autoimmune reactions;
sensitive individuals more likely to have allergies, asthma, autoimmune-like
symptoms, especially rheumatoid-like ones |
More likely to have allergies and asthma; familial
presence of autoimmune diseases, especially rheumatoid arthritis; IgA
deficiencies |
|
Can produce an immune response in CNS |
On-going immune response in CNS |
|
Causes brain/MBP autoantibodies |
Brain/MBP autoantibodies present |
|
Causes overproduction of Th2 subset; kills/inhibits
lymphocytes, T-cells, and monocytes; decreases NK T-cell activity; induces or
suppresses IFNg & IL-2 |
Skewed immune-cell subset in the Th2 direction; decreased
responses to T-cell mitogens; reduced NK T-cell function; increased IFNg
& IL-12 |
|
CNS Structural Pathology |
|
|
Selectively targets brain areas unable to detoxify or
reduce Hg-induced oxidative stress |
Specific areas of brain pathology; many functions spared |
|
Damage to Purkinje and granular cells |
Damage to Purkinje and granular cells |
|
Accummulates in amygdala and hippocampus |
Pathology in amygdala and hippocampus |
|
Causes abnormal neuronal cytoarchitecture; disrupts
neuronal migration & cell division; reduces NCAMs |
Neuronal disorganization; increased neuronal cell
replication, increased glial cells; depressed expression of NCAMs |
|
Progressive microcephaly |
Progressive microcephaly and macrocephaly |
|
Brain stem defects in some cases |
Brain stem defects in some cases |
|
Abnormalities in Neuro-chemistry |
|
|
Prevents presynaptic serotonin release & inhibits
serotonin transport; causes calcium disruptions |
Decreased serotonin synthesis in children; abnormal
calcium metabolism |
|
Alters dopamine systems; peroxidine deficiency in rats
resembles mercurialism in humans |
Possibly high or low dopamine levels; positive response to
peroxidine (lowers dopamine levels) |
|
Elevates epinephrine & norepinephrine levels by
blocking enzyme that degrades epinephrine |
Elevated norepinephrine and epinephrine |
|
Elevates glutamate |
Elevated glutamate and aspartate |
|
Leads to cortical acetylcholine deficiency; increases
muscarinic receptor density in hippocampus & cerebellum |
Cortical acetylcholine deficiency; reduced muscarinic
receptor binding in hippocampus |
|
Causes demyelinating neuropathy |
Demyelination in brain |
|
EEG Abnormalities / Epilepsy |
|
|
Causes abnormal EEGs, epileptiform activity |
Abnormal EEGs, epileptiform activity |
|
Causes seizures, convulsions |
Seizures; epilepsy |
|
Causes subtle, low amplitude seizure activity |
Subtle, low amplitude seizure activities |
|
Population Characteristics |
|
|
Effects more males than females |
Male:female ratio estimated at 4:1 |
|
At low doses, only affects those geneticially susceptible |
High heritability - concordance for MZ twins is 90% |
|
First added to childhood vaccines in 1930s |
First "discovered" among children born in 1930s |
|
Exposure levels steadily increased since 1930s with rate
of vaccination, number of vaccines |
Prevalence of autism has steadily increased from 1 in 2000
(pre1970) to 1 in 500 (early 1990s), higher in 2000. |
|
Exposure occurs at 0 - 15 months; clinical silent stage
means symptom emergence delayed; symptoms emerge gradually, starting with
movement & sensation |
Symptoms emerge from 4 months to 2 years old; symptoms
emerge gradually, starting with movement & sensation |
Autism
Autism, or Autistic Spectrum Disorder (ASD), is considered a neurodevelopmental
syndrome, emerging early in life and exhibiting a constellation of seemingly
unrelated features and a wide variation in symptom expression and level of
severity by individual (Filipek et al, 1999; Bailey et al, 1996). The
diagnostic criteria for autism are qualitative impairments in social
relatedness, deficits in verbal and nonverbal communication, and the presence
of repetitive and restricted behaviors or interests (APA, 1994). As will be
cited below, other traits associated with autism are movement disorder, sensory
dysfunction, and cognitive impairments as well as gastrointestinal difficulties
and immune abnormalities (Gillberg & Coleman, 1992; Warren et al, 1990;
Horvath et al, 1999). Onset must occur before age 36 months (APA, 1994);
although in some instances deficits are apparent at birth, in the great
majority of cases there are at least several months of normal development
followed by clear regression or failure to progress normally (Gillberg &
Coleman, 1992; Filipek et al, 1999; Bailey et al, 1996). Formerly regarded as a
rare disease, autism is now said to affect one in 500 children (Bristol et al,
1996), with some estimates suggesting one in 100 for a broader phenotype often
labeled as the "autism-spectrum" of disorders and which includes both
higher and lower functioning individuals (Arvidsson et al, 1997; Wing, 1996).
Autism and autistic symptoms can arise from a number of known disorders,
most notably tuberous sclerosis, Rhett syndrome, Landau-Kleffner syndrome,
Fragile X, Phenylketonuria, purine autism, and other purine metabolic diseases
such as PRPP synthetase defects and 5'-nucleotidase superactivity. The etiology
and pathogenesis of the vast majority of autism cases - 70% - 90% (Gillberg and
Coleman, 1992; Bailey et al, 1996) - remain unexplained, however, despite ASD
being "one of the most extensively studied disorders in child psychiatry
today" (Malhotra and Gupta, 1999). Nevertheless, there is general
agreement that most cases of autism arise "from the interaction of an
early environmental insult and a genetic predisposition" (Trottier et al,
1999; Bristol et al, 1996).
Mercury
A heavy metal, mercury (Hg) is widely considered one of the most toxic
substances on earth (Clarkson, 1997). Instances of Hg poisoning or
"mercurialism" have been described since Roman times. The Mad Hatter
in Alice in Wonderland was a victim of occupational exposure to mercury
vapor, referred to as "Mad Hatter's Disease." Further human data has
been derived from instances of widespread poisonings during the 20th Century.
These misfortunes include an outbreak in Minamata, Japan, caused by consumption
of contaminated fish and resulting in "Minamata Disease;" outbreaks
in Iraq, Guatemala and Russia due to ingestion of contaminated seed grains;
and, in the first half of the century, poisoning of infants and toddlers by
mercury in teething powders, leading to acrodynia or Pink Disease. Besides
these epidemics, numerous instances of individual or small group cases of Hg
intoxication and subsequent phenotype are described in the literature.
The constellation of mercury-induced symptoms varies enormously from
individual to individual. The diversity of disease manifestations derives from
a number of interacting variables which are summarized in Table I. The
variables which affect phenotype include an individual's age, the total dosage,
dose rate, duration of exposure, type of mercury, routes of exposure such as
inhaled, subcutaneous, oral, or intramuscular, and, most importantly, by
individual sensitivity arising from immune and genetic factors (Dales, 1972;
Koos and Longo, 1976; Matheson et al, 1980; Eto et al, 1999; Feldman, 1982;
Warkany and Hubbard, 1953).
Table I: Summary
of Mercury Exposure Variables
Leading to Diverse & Non-Specific Symptomatology
|
Variable |
Level of
Variable |
|
Exposure Amount |
Ranges from high doses, leading to death or near death
with severe impairments, to low "safe" doses, leading to subtle
neurological and other physical impairments |
|
Duration of exposure |
One time vs. multiple times over the course of weeks,
months, or years |
|
Dose rate |
Bolus dose, daily dose |
|
Individual sensitivity |
A function of (a) the age at which exposure occurs, that
is, prenatal, infant, child, adolescent, or adult, (b) genetically determined
reactivity to mercury, and (c) gender |
|
Common types of mercury |
The organic alkyl forms - methylmercury and ethylmercury;
and inorganic forms - metallic mercury, elemental (liquid) mercury, and ionic
mercury/mercuric salt |
|
Primary routes of exposure |
Inhalation of mercury vapors, orally through the
intestinal tract, subcutaneous and intramuscular injections, topically
through ear drops, teething powders, skin creams and ointments, and
intravenously during medical treatments |
While these variations in exposure, individual status, and genotype give
rise to a diverse clinical phenotype, there are nevertheless obvious
commonalities across all mercury-caused disorders. Thus, for example, victims
will almost always develop a movement disorder, but in some individuals this
may manifest as mere clumsiness, while others will develop severe involuntary
jerking movements. Likewise, psychological disturbances are usually present,
but in some individuals these might manifest as anxiety while in others it
might present as aggression or irritability.
Diagnosing Mercury Poisoning in Autism
Mercury poisoning can be difficult to diagnose and is often interpreted by
clinicians as a psychiatric disorder, especially if exposure is not suspected
(Diner and Brenner, 1998; Frackelton and Christensen, 1998). The difficulty in
diagnosis derives primarily from two notable characteristics of this heavy
metal. First, there can be a long latent period between time of exposure and
onset of overt symptoms, so that the connection between the two events is often
overlooked. The latency period is discussed in more detail below. Second, the
diverse manifestations of the disease make it difficult for the clinician to
find a precise match of his particular patient's symptoms with those described
in other case reports (Adams et al, 1983, Kark et al, 1971; Florentine and
Sanfilippo, 1991; Matheson et al, 1980; Frackelton and Christensen, 1998;
Warkany & Hubbard, 1953).
Due to the difficulty of diagnosing mercurialism based on presentation of
non-specific symptoms alone, clinicians have come to rely on the following
criteria (Warkany & Hubbard, 1953; Vroom and Greer, 1972).
1. Observation of impairments in
many but not all of the following domains: (a) movement/motor disorder, (b)
sensory abnormalities, (c) psychological and behavioral disturbances, (d)
neurological and cognitive deficits, (e) impairments in language, hearing, and
vision, and (f) miscellaneous physical presentations such as rashes or unusual
reflexes (Adams et al, 1983; Snyder, 1972; Vroom & Greer, 1972).
2. Known exposure to Hg (a) at a level that has
been documenting as causing impairment in similar individuals under similar
circumstances, and (b) at approximately the same time as the symptoms emerge, with
allowances given for the latency period (Ross et al, 1977; Amin-Zaki et al,
1978). It should be noted that the dose which is considered "toxic"
vs. "safe" is unresolved among toxicologists; some researchers feel
that any amount of exposure is "unsafe" (see EPA, 1997, pp.6-47 to
6-59, for dose discussion).
3. Detectable levels of mercury in urine, blood, or
hair (Florentine and Sanfilippo, 1991; Frackelton and Christensen, 1998; EPA,
1997, p.ES-2). Importantly, because mercury can clear from biologic samples
before the patient feels symptoms or is tested, the lack of detectable mercury
is not cause for ruling out mercury poisoning; and conversely, detectable
levels have been observed in unaffected individuals (Adams et al, 1983; Warkany
& Hubbard, 1953; Cloarec, 1995).
4. Improvement in symptoms after chelation. While
many patients' symptoms resolve with chelation, some clearly poisoned
individuals do not improve. Other exposed subjects have also been known to
improve without intervention (Vroom & Greer, 1972; Warkany & Hubbard,
1953).
Thus, none of these criteria is sufficient on its own for a
certain diagnosis. Rather, observed effects within two or three domains are
generally required. This paper, which reviews and compares the extensive
literature available on both ASD and mercury, provides citations documenting
that, based on these four diagnostic criteria, many if not most cases of autism
meet the requirements for mercury poisoning. In fact, this review and its
citations (i) delineate a single mechanism for inducing all of the primary
domains of impairment and biological abnormalities in autism, including its
genetic component, prevalence levels, and sex ratios; and (ii) identify that
mechanism as arising from the "environmental insult" of early
childhood exposure to mercury. Furthermore, the route of exposure is
thimerosal, which is 50% ethylmercury by weight and which is a preservative
used in many childhood vaccines.
We are not suggesting that the previous reports of mercurialism described in
the literature are in fact cases of autism; rather, we claim that autism
represents its own unique form of Hg poisoning, just like acrodynia, Minamata
disease, and Mad Hatter's disease represent distinct yet closely related
presentations of mercurialism. A unique expression would be expected in cases
of autism, given that the effects of repeated vaccinal administration of
ethylmercury to infants and toddlers have never been described before in
mercury-related literature. We maintain that the diverse phenotype that is
autism matches the diverse phenotype that is mercurialism to a far greater
degree that could reasonably be expected to occur by chance. Given the known
exposure to mercury via vaccination of autistic children and the presence of
mercury found in biologic samples from a number of autistic subjects, also
described here, we are confident that our claim is substantiated. Our paper
discusses some important medical and societal ramifications of this conclusion.
The overt symptoms of ASD and mercury poisoning, described in the literature
and presented here, are strikingly similar. Summary tables have been provided
after each section to aid in symptom comparisons.
a. Affect/Psychological Presentation
Since its initial description in 1943 by Leo Kanner, a psychiatrist, autism has
been defined primarily as a psychiatric condition. One of the three
requirements for diagnosis is a severe deficit in social interactions (APA,
1994). Self and parental reports describe children and adults who prefer to be
alone and who will withdraw to their rooms if given the chance (MAAP,
1996-1999). Even high functioning autistics tend to be aloof, have poor social
skills, are unable to make friends, and find conversation difficult (Tonge et
al, 1999; Capps et al, 1998). Face recognition and what psychologists call
"theory of mind" are impaired (Klin et al, 1999, Baron-Cohen et al,
1993). Poor eye contact or gaze avoidance is present in most cases, especially
in infancy and childhood (Bernabei et al, 1998).
The second psychobehavioral diagnostic characteristic of autism is the
presence of repetitive, stereotyped activities and the need for sameness (APA,
1994). Traits in this domain strongly resemble obsessive-compulsive tendencies
in both thought and behavior (Lewis, 1996; Gillberg & Coleman, 1992, p.27),
especially as the individual becomes more high functioning (Roux et al, 1998):
"it [is] very difficult.to distinguish between obsessive ideation and the
bizarre preoccupations so commonly seen in autistic individuals" (Howlin,
2000). Serotonin uptake inhibitors known to be effective for OCD also reduce
repetitive behaviors in some autistic patients (Lewis, 1996). Most autistic
subjects - 84% in one study - show high levels of anxiety and meet diagnostic criteria
for anxiety disorder (Muris et al, 1998).
ASD has been linked to depression, based on symptoms, familial history of
depression and the positive response to SSRIs among many autistics (Clarke et
al, 1999; DeLong, 1999; Piven and Palmer, 1999). One subset of autistics has
been described as "passive", with flat affect, "absence of
facial expression," lack of initiative, and diminished outward emotional
reactions. Some autistics have a strong family history of manic depression and
mood swings, and, among those who are verbal, psychotic talk is frequently
observed (Plioplys, 1989). Autism is also said to strongly resemble childhood
schizophrenia. In the past it was often misdiagnosed as such (Gillberg &
Coleman, 1992, p.100), and there are a number of instances of dual
ASD-schizophrenia diagnoses in the literature (Clarke et al, 1999).
Furthermore, irrational fears, aggressive behaviors, and severe temper tantrums
are common (Muris et al, 1998; McDougle et al, 1994), as are chronic
hyperarousal and irritability (Jaselskis et al, 1992). "Inexplicable
changes of mood can occur, with giggling and laughing or crying for no apparent
reason" (Wing & Attwood, 1987).
Mercury poisoning, when undetected, is often initially diagnosed as a
psychiatric disorder in both children and adults (Fagala and Wigg, 1992).
Common psychiatric symptoms are (a) depression, including "lack of
interest" and "mental confusion;" (b) "extreme
shyness," indifference to others, active avoidance of others or "a
desire to be alone"; (c) irritability in adults and tantrums in children;
and (d) anxiety and fearfulness. Neurosis, including schizoid and
obsessive-compulsive traits, has been reported in a number of cases (Fagala and
Wigg, 1992; Kark et al, 1971; O'Carroll et al, 1995; Florentine and Sanfilippo,
1991; Amin-Zaki, 1974 and 1979; Matheson et al, 1980; Joselow et al, 1972;
Smith, 1972; Lowell, 1996; Tuthill, 1899; Clarkson, 1997; Camerino et al, 1981;
Grandjean et al, 1997; Piikivi et al, 1984; Rice, 1996; Vroom & Greer,
1972; Adams et al, 1973; Hua et al, 1996).
Juvenile monkeys prenatally exposed to mercury exhibit decreased social play
and increased passive behavior (Gunderson et al, 1986, 1988), as well as
impaired face recognition (Rice, 1996). Humans exposed to mercury vapor also
perform poorly on face recognition tests and may present with a "mask
face" (Vroom & Greer, 1972); emotional instability can occur in
children and adults exposed to Hg. For instance, Iraqi children poisoned by
methylmercury had a tendency "to cry, laugh, or smile without obvious
provocation" (Amin-Zaki et al, 1974 & 1979), like the autistic group
described by Wing and Attwood (1987).
Table II: Summary
of Psychiatric Disturbances
Found in Autism & Mercury Poisoning
|
Mercury
Poisoning |
Autism |
|
Extreme shyness, social withdrawal, feeling overly
sensitive, introversion |
Social deficits, social withdrawal, self reports of
extreme shyness, aloofness |
|
Mood swings; flat affect; mask face; laughing or crying
without provocation; episodes of hysteria |
Mood swings; flat affect in some; no facial expression;
laughing or crying without reason |
|
Anxiety; nervousness; tremulousness; somatization of
anxious feelings |
Anxiety, nervousness; anxiety disorder |
|
Schizoid tendencies, neurosis, obsessive-compulsive
traits, repetitive dreams |
Schizophrenic traits; OCD traits; repetitive behaviors and
thoughts |
|
Lack of eye contact; being less talkative; hesitancy to
engage others |
Lack of eye contact, gaze avoidance; avoids conversation |
|
Depression, lack of interest in life, lassitude, fatigue,
apathy; feelings of hopelessness; melancholy |
Association with depression; lack of initiative,
diminished outward emotions |
|
On the one hand, less overtly active, unwilling to go
outside or be with others; on the other hand, increased restlessness |
Tendency to withdraw, especially to own rooms, prefer to
be alone; hyperactivity |
|
Irrational fears |
Irrational fears |
|
Irritability, anger, and aggression; in children this may
manifest as frequent and severe temper tantrums |
Irritability and aggression; severe temper tantrums in
children |
|
Psychotic episodes; hallucinations, hearing voices;
paranoid thoughts |
Psychotic talk, paranoid thoughts |
|
Impaired face recognition |
Impaired face recognition |
Since traditionally autism has been characterized and studied by researchers
primarily in psychiatric terms, providing case studies illustrating the psychiatric
aspects of ASD and of mercurialism are necessary in establishing the
similarities of the two disorders on this critical domain. Also included is a
comparison of "Lenny," an autistic adult described by Rhea Paul
(1987), and the Mad Hatter from Alice in Wonderland, considered to be an
accurate portrayal of victims of the disease. Of particular relevance in all
these cases are social withdrawal and deficits in social communication, traits
(i) always prominent in autism and (ii) clearly associated with mercurialism.
Case Studies: Autism
"I am 18 years old. My parents found out I was autistic when I was 18
months old. My parents said I banged my head a lot when I got frustrated when I
was young. Head banging motions help me deal with nervousness. I also take 2
medications to help me cope with stress. I have very few friends. It is also
somewhat painful for me to look people in the eye. This sometimes makes people
think I am not paying attention" (The MAAP, Vol. II, 1997).
"I have a high-functioning autistic
eight-year-old boy. My mistake was putting him in the second grade with a
teacher who was determined to 'socialize' him. After three months, the anxiety
proved to be too great for him. He spent a lot of time crying, withdrawing to
his room, becoming compulsive and belligerent. In another era, he would have
been seen as having a 'nervous breakdown'" (The MAAP, Vol. II, 1997).
"I am writing regarding our 25 year old son
who was diagnosed only a few months ago as having Asperger's Syndrome. All his
life he displayed the 'classic' symptoms of Asperger's (lack of social skills,
disorganization, anxiety, etc.). A few months ago, he became clinically
depressed, phobic about being around people for fear of more rejection or being
laughed at. He now has obsessive thoughts that our home is electronically
'bugged' and all his actions are being observed and belittled" (The MAAP,
Vol. II, 1997).
"Several people have asked me what it's like
to have Asperger's Syndrome. Today, I still prefer to work on my computer or
with electronics rather than socialize. I've never been able to tolerate any
kind of physical contact or intimacy. I like wrestling and rough-housing, but I
hate being caressed or held." (The MAAP, Vol. II, 1997).
"My son Brian is a 6-year-old with high
functioning autism. Our main problem now is his rigidity and
obsessive/compulsive behaviors. He gets extremely upset when activities don't
go as he thinks they should. He first gets mad, screaming and yelling, then
begins to obsessively talk about how he can remedy the situation, then often
begins to cry uncontrollably. These tantrums can go on for hours" (The
MAAP, Vol. IV, 1996).
"[I'm] age 12r. I have Autism/PDD. I don't
really know any real social skills, though my brother Isaiah says I am a social
outcast. I do have trouble making new friends because I get real shy and
nervous" (The MAAP, Vol. IV, 1997).
"I am the mother of three autistic boys. Nate
was considered very shy. Poor eye contact but very smart and doing well in
school. Nate was also diagnosed with Hypotonia of the face (which answered all
the mumbling he did wasn't just shyness) and extremities" (The MAAP, Vol.
III, 1999)
"I spent many hours sitting in the trees or
under the bed or in a dark closet. I had a loud flat voice. Socialization has
always been beyond me" (The MAAP, Vol. II, 1998).
"I sit in my room a prisoner to my autism. Mom
and sis doing their loving best to get me out. I wanted to get out - really get
out. I wanted to love, to feel, to connect. But, I couldn't. I was stuck. I was
slowly dying. There were days I truly wanted to end it all. If any days were
good, I didn't deserve it. I shouldn't be happy. Autism teaches you that -
because it's a life sentence" (The MAAP, Vol. VI, 1996).
Case Studies: Mercury Poisoning
A 12 year old girl with recent mercury vapor poisoning was initially diagnosed
as having a psychiatric disturbance. Her behavior was more normal when she was
unaware of being watched. She became upset when people were around, was
reluctant to speak when others were present, spoke in a soft, mumbling voice,
lacked eye contact, had a flat affect, was sometimes tearful, experienced
auditory hallucinations of voices laughing at her, wished to stay alone in her
room with the lights off and her head covered, and had frequent temper tantrums
(Fagala and Wigg, 1992).
Sufferers of Mad Hatter's disease, arising from
prolonged mercury vapor exposure, were known to suffer from depression,
lassitude, acute anxiety, and irrational fears. They also became nervous,
timid, and shy. They blushed readily, were embarrassed in social situations,
objected to being watched, and sought to avoid people. They felt a constant
impulse to return home. They were easily upset, and were prone to agitation,
irritability, anger, and aggressive behavior (O'Carroll et al, 1995).
A survey on an Internet site of adult acrodynia
victims, which compared the symptoms of adults who suffered from acrodynia as
children with controls, reported the following symptoms as seen to a greater
degree in acrodynia sufferers than in controls: dislikes being touched or
hugged, is a loner, lacks self confidence, feels nervousness and has a racing
heart, has depression and suicidal feelings (Farnesworth, 1997). One acrodynia
victim described his own situation: "not having learnt normal social
skills I spent a lot of my time alone.Gradually by age 11 or so, I was becoming
'normal'.But, I have never overcome the headache problem, irritability, shyness
with real people, not wanting to be touched, depression, fear of doctors, great
anxiety." (Neville's Recollection, Pink Disease site)
A doctor from the 19th century described several
cases of mercury poisoning from dental amalgams: "There is mental
excitability as well as mental depression; perplexing events cause the highest
degree of excitement, ordinary conversation sometimes causes complete
confusion, headache, palpitation, intense solicitude, and anxiety, without
reason for it. Such are some of the symptoms attending these cases." As an
example he cites the case of a young woman who "had come to be melancholic
and to withdraw herself from her family and friends, seeking the seclusion of
her room -- refusing to go out or to associate with others, or even with the
members of her own household." (Tuthill, 1899)
Nearly a century later, initial questioning of a 28
year old woman, subsequently found to have mercury vapor poisoning,
"elicited the fact that she had become increasingly withdrawn from social
activities and had felt most uncomfortable when with strangers. She also felt
that her friends had turned against her. She had a repetitive disturbing dream
of electric fire around the frames of the windows in her bedroom." (Ross
et al, 1977)
Lenny and The Mad Hatter
(a) Rigid literal interpretation of word meaning; word meaning and pragmatic
errors which interfere with social communication
Lenny -
"He was very literal minded, and words spoken to him became matters of
immutable fact. For example, he was trying on new shoes. His mother asked him
if they slipped up and down. He said they didn't, and when asked again if he
were sure, he replied, 'No, they don't slip up and down; they slip down and then
they slip up.' "
The Mad Hatter -
"Take some more tea," the March Hare said to Alice, very earnestly.
"I've had nothing yet," Alice replied in an offended tone: "so I
ca'n't take more."
"You mean you ca'n't take less," said the Hatter: "It's very
easy to take more than nothing."
(b) Social deficits, inability to interpret
social rules, leading to perceived rude behavior
Lenny -
"Although he tried working in his father's business for a time, his
immaturity, self-centered behavior, and lack of social judgment required his
return to a sheltered setting."
The Mad Hatter - "Your hair wants
cutting," said the Hatter. He had been looking at Alice for some time with
great curiosity, and this was his first speech.
"You should learn not to make personal remarks," Alice said with some
severity: "it's very rude."
The Hatter opened his eyes wide upon hearing this; but all he said was
"Why is a raven like a writing desk?"
(c) Inability to engage in meaningful social
conversation; poor conversational interpretation skills; perseverative thoughts
Lenny - "During one interview he
engaged in a 20 minute monologue about a broken washing mashine. The
interviewer momentarily dozed off. Upon rousing, the interviewer exclaimed,
'Oh, Lenny, I'm sorry!' 'It's all right,' Lenny replied calmly, 'the washing
machine got fixed."
"What a funny watch!" she remarked. "It tells the day of the
month, and doesn't tell what o'clock it is!"
"Why should it?" muttered the Hatter. "Does your watch
tell you what year it is?"
"Of course not, " Alice replied very readily: "but that's
because it stays the same year for such a long time altogether."
"Which is just the case with mine," said the Hatter.
Alice felt dreadfully puzzled. The Hatter's remark seemed to her to have no
sort of meaning in it, and yet it was certainly plain English.
b. Language and Hearing
The third diagnostic criterion for autism is a qualitative impairment in
communication (APA, 1994), and such impairment is a primary feature of mercury
poisoning.
Delayed language onset is often among the first overt signs of ASD
(Eisenmajer et al, 1998). Historically, half of those with classic autism
failed to develop meaningful speech (Gillberg & Coleman, 1992; Prizant,
1996); and oral-motor deficits (e.g. chewing, swallowing) are often present
(Filipek et al, 1999). When speech develops, there may be "specific
neuromotor speech disorders," including verbal dyspraxia, a dysfunction in
the ability to plan the coordinated movements to produce intelligible sequences
of speech sounds, or dysarthria, a weakness or lack of control of the oral
musculature" leading to articulation problems (Filipek et al, 1999).
Echolalic speech and pronoun reversals are typically found in younger children.
Many ASD subjects show poorer performance on tests of verbal IQ relative to
performance IQ (Dawson, 1996; Filipek at al, 1999). Higher functioning
individuals, such as those with Asperger's Syndrome, may have language fluency
but still exhibit semantic (word meaning) and pragmatic (use of language to
communicate) errors (Filipek et al, 1999).
Auditory impairment is also common. Two separate studies, for example, both
found that 24% of autistic subjects have a hearing deficit (Gillberg &
Coleman, 1992). More recently Rosenhall et al (1999) have diagnosed hearing
loss ranging from mild to profound, as well as hyperacusis, otitis media, and
conductive hearing loss, in a minority of ASD subjects, and these traits were
independent of IQ status. Among the earliest signs of autism noted by mothers
were strange reactions to sound and abnormal babble (Gillberg & Coleman,
1992), and many ASD children are tested for deafness before receiving a formal
autism diagnosis (Vostanis et al, 1998). "Delayed or prompted response to
name" differentiates 9-12 months old toddlers, later diagnosed with
autism, from mentally retarded and typical controls (Baranek, 1999). In fact,
"bizarre responses" to auditory stimuli are nearly universal in
autism and may present as "either a lack of responsiveness or an exaggerated
reaction to auditory stimuli" (Roux et al, 1998), possibly due to sound
sensitivity (Grandin, 1996). Kanner noted an aversion to certain types of
sounds, such as vacuum cleaners (Kanner, 1943). Severe deficits in language
comprehension are often present (Filipek et al, 1999). Difficulties in picking
out conversational speech from background noise are commonly reported by high
functioning ASD individuals (Grandin, 1995; MAAP, 1997-1998).
In regard to language and auditory phenomena, autism's parallels to
mercurialism are striking. Emerging signs of mercury poisoning are dysarthria
(defective articulation in speech due to CNS dysfunction) and then auditory
disturbance, leading to deafness in very high doses (Clarkson, 1992). In some
cases, hearing impairment manifests as an inability to comprehend speech rather
than an inability to hear sound (Dales, 1972). Hg poisoning can also result in
aphasia, the inability to understand and/or physically express words (Kark et
al, 1971). Speech difficulties may arise from "intention tremor, which can
be noticeable about the mouth, tongue, face, and head, as well as in the
extremities" (Adams et al, 1983).
Mercury-exposed children especially show a marked difficulty with speech
(Pierce et al, 1972; Snyder, 1972; Kark et al, 1971). Even children exposed
prenatally to "safe" levels of methylmercury performed less well on
standardized language tests than did unexposed controls (Grandjean et al,
1998). Iraqi babies exposed prenatally either failed to develop language or
presented with severe language deficits in childhood. They exhibited
"exaggerated reaction" to sudden noise and some had reduced hearing
(Amin-Zaki, 1974 and 1979). Iraqi children who were postnatally poisoned from
bread containing either methyl or ethylmercury developed articulation problems,
from slow, slurred word production to the inability to generate meaningful
speech. Most had impaired hearing and a few became deaf (Amin-Zaki, 1978). In
acrodynia, symptoms of sufferers (vs. controls) include noise sensitivity and
hearing problems (Farnesworth, 1997).
Adults also exhibit these same Hg-induced impairments. There is slurred or
explosive speech (Dales, 1972), as well as difficulty in picking out one voice
from a group (Joselow et al, 1972). Poisoned Iraqi adults developed
articulation problems (Amin-Zaki, 1974). A 25 year old man with elemental
mercury poisoning had reduced hearing at all frequencies (Kark et al, 1971).
Thimerosal injected into a 44 year old man initially led to difficulty
verbalizing, even though his abilities in written expression were
uncompromised; he then progressed to slow and slurred speech, although he could
still comprehend verbal language; and he finally lost speech altogether (Lowell
et al, 1996). In Mad Hatter's disease, there were word retrieval and
articulation difficulties (O'Carroll et al, 1995). A scientist who recently
died from dimethylmercury poisoning demonstrated an inability to understand
speech despite having good hearing sensitivity for pure tones (Musiek and
Hanlon, 1999). Workers exposed to mercury vapor showed decreased verbal
intelligence relative to performance IQ (Piikivi et al, 1984; Vroom and Greer,
1972)
.
Table III: Summary
of Speech, Language
& Hearing Deficits in Autism & Mercury Poisoning
|
Mercury
Poisoning |
Autism |
|
Complete loss of speech in adults or children; failure to
develop speech in infants |
Delayed language onset; failure to develop speech |
|
Dysarthria; speech difficulties from intention tremor;
slow and slurred speech |
Dysarthria; dyspraxia and oral-motor planning
difficulties; unintelligible speech |
|
Aphasia, the inability to use or understand words,
inability to comprehend speech although ability to hear sound is intact |
Speech comprehension deficits, although ability to hear
sound is intact |
|
Difficulties verbalizing; word retrieval problems |
Echolalia; pronoun reversals, word meaning and pragmatic
errors; limited speech production |
|
Auditory disturbance; difficulties differentiating voices
in a crowd |
Difficulties following conversational speech with
background noise |
|
Sound sensitivity |
Sound sensitivity |
|
Hearing loss; deafness in very high doses |
Mild to profound hearing loss |
|
Poor performance on standardized language tests |
Poor performance on verbal IQ tests |
c. Sensory Perception
Sensory impairment is considered by many researchers to be a defining
characteristic of autism (Gillberg and Coleman, 1992; Williams, 1996). Baranek
(1999) detected sensory-motor problems - touch aversion, poor non-social visual
attention, excessive mouthing of objects, and delayed response to name - in
9-12 month old infants later diagnosed with autism, and suggests that these
impairments both underlie later social deficits and serve to differentiate ASD
from mental retardation and typical controls. Besides sensitivity to sound, as
previously noted, ASD often involves insensitivity to pain, even to a burning
stove (Gillberg & Coleman, 1992), while on the other hand there may be an
overreaction to stimuli, so that even light to moderate touches are painful.
Pinprick tests are usually normal. Children with autism have been described as
"stiff to hold," and one of the earliest signs reported by mothers is
an aversion to being touched (Gillberg & Coleman, 1992). Abnormal sensation
in the extremities and mouth are common. Toe-walking is frequently seen. Oral
sensitivity often results in feeding difficulties (Gillberg & Coleman,
1992, p.31). Autistic children frequently have vestibular impairments and
difficulty orienting themselves in space (Grandin, 1996; Ornitz, 1987).
As in ASD, sensory issues are reported in nearly all cases of mercury
toxicity, and serve to demonstrate the similarities between the two conditions.
Paresthesia, or abnormal sensation, tingling, and numbness around the mouth and
in the extremities, is the most common sensory disturbance in Hg poisoning, and
is usually the first sign of toxicity (Fagala and Wigg, 1992; Joselow et al,
1972; Matheson et al, 1980; Amin-Zaki, 1979). In Japanese who ate contaminated
fish, there was numbness in the extremities, face and tongue (Snyder, 1972;
Tokuomi et al, 1982). Iraqi children who ate bread experienced sensory changes
including numbness in the mouth, hands and feet, and a feeling that there were
"ants crawling under the skin." These children could still feel a
pinprick (Amin-Zaki, 1978). Loss of position in space has also been noted
(Dales, 1972). Acrodynia sufferers describe excessive pain when bumping limbs,
numbness, and poor circulation (Farnesworth, 1997). One adult acrodynia victim
described himself as a boy as "shying away from people wanting to touch
me" due to extreme touch sensitivity (Neville Recollection, Pink Disease
Support Group). Iraqi babies exposed to mercury prenatally showed excessive
crying, irritability, and exaggerated reaction to stimulation such as sudden
noise or when touched (Amin-Zaki et al, 1974 and 1979).
Table IV: Summary
of Sensory Abnormalities
in Mercury Poisoning & Autism
|
Mercury
Poisoning |
Autism |
|
Abnormal sensation or numbness around mouth and
extremities (paresthesia); burning feet |
Abnormal sensation in mouth and extremities; excessive
mouthing of objects (infants); toe walking; difficulty grasping objects |
|
Sound sensitivity |
Sound sensitivity |
|
Excessive pain when bumping; abnormal touch sensations;
touch aversion |
Insensitivity or overreaction to pain and touch; touch
aversion; stiff to hold |
|
Loss of position in space |
Vestibular system abnormalities; difficulty orienting self
in space |
|
Normal pinprick tests |
Normal pinprick tests |
d. Movement/Motor Function
Nearly all cases of autism include disorders of physical movement. Movement
disturbances have been detected in infants as young as four to six months old
who were later diagnosed as autistic: Teitelbaum et al (1998) have observed
that these children do not lie, roll over, sit up or crawl like normal infants;
impairment in motor control sometimes caused these babies to fall over while
sitting, consistently to avoid using one of their arms, or to rest on their
elbows for stability while crawling. Later, when trying to walk their gait was
abnormal, and some degree of asymmetry, mostly right-sided, was present in all
cases studied. Kanner noted in several of his subjects the absence of crawling
and a failure to assume an anticipatory posture preparatory to being picked up
in infancy (Kanner, 1943). Arm flapping, abnormal posture, jumping, and
hand-finger mannerisms (choreiform movements) are common (Tsai, 1996). Many
individuals with Asperger's syndrome are typically characterized as
uncoordinated or clumsy (Kugler, 1998). Other autism movement disorders include
praxis (problems with intentional movement), stereotypies, circling or
spinning, rocking, toe walking, myoclonal jerks, difficulty swallowing and
chewing, difficulty writing with or even holding a pen, limb apraxia, and poor
eye-hand coordination (Caesaroni and Garber, 1991; Gillberg and Coleman, 1992; Filipek
et al, 1999).
Like ASD, movement disorders have been a feature of virtually all
descriptions of mercury poisoning in humans (Snyder, 1972). Even children
prenatally exposed to "safe" levels of methylmercury had deficits in
motor function (Grandjean et al, 1998). The movement-related behaviors are
extremely diverse: Iraqi infants and children exposed postnatally, for example,
developed ataxia that ranged from clumsiness and gait disturbances to an
"inability to stand or even sit" (Amin-Zaki et al, 1978). The various
movement behaviors are listed more fully in Table V (Adams et al, 1983; Kark et
al, 1971; Pierce et al, 1972; Snyder, 1972; O'Carroll et al, 1995; Tokuomi et
al, 1982; Amin-Zaki, 1979; Florentine and Sanfilippo, 1991; Rohyans et al, 1984;
Fagala and Wigg, 1992; Smith, 1977; Grandjean et al, 1998; Farnesworth, 1997;
Dales, 1972; Matheson et al, 1980; Lowell et al, 1996; O'Kusky et al, 1988;
Vroom and Greer, 1972; Warkany and Hubbard, 1953).
Noteworthy because of similarities to movement disorders in autism are
reports in the Hg literature of (a) an infant with "peculiar tremulous
movements of the extremities which were principally proximal and can best be
described as flapping in nature" (Pierce et al, 1972; Snyder, 1972); (b) "jerking
movements of the upper extremities" in a man injected with thimerosal
(Lowell et al, 1996); (c) "constant choreiform movements affecting the
fingers and face" in mercury vapor intoxication (Kark et al, 1971); (d)
myoclonal jerks, associated with epilepsy among Iraqi subjects (Amin-Zaki et
al, 1978); (e) poor coordination and clumsiness among victims of acrodynia
(Farnesworth, 1997); (f) rocking among infants with acrodynia (Warkany and
Hubbard, 1953); (g) "unusual postures" observed in both acrodynia and
mercury vapor poisoning (Vroom and Greer, 1972; Warkany and Hubbard, 1953); and
(h) toe walking among less severely poisoned children in the Minamata epidemic
(Minamata Disease, 1973). In animal studies, cats exposed to mercury by
eating fish developed "circling movements" (Snyder, 1972), and
subcutaneous administration of methylmercury to rats during postnatal
development has resulted in postural disorders (O'Kusky et al, 1988).
As summarized in Table V, movement similarities in autism and Hg poisoning
are clear.
Table V: Summary
of Motor Disorder Behaviors
in Mercury Poisoning & Autism
|
Mercury
Poisoning |
Autism |
|
Involuntary jerking movements, e.g., arm flapping, ankle
jerks, myoclonal jerks; choreiform movements; circling (cats); rocking;
purposeless movement of extremities; twitching, shaking; muscular spasticity |
Stereotyped movements such as arm flapping, jumping,
circling, spinning, rocking; myoclonal jerks; choreiform movements |
|
Unsteadiness in handwriting or an inability to hold a pen;
deficits in eye-hand coordination; limb apraxia; intention tremors; loss of
fine motor skills |
Difficulty in writing with or holding a pen; poor eye-hand
coordination; limb apraxia; problems carrying out intentional movements
(praxia) |
|
Ataxia: gait impairment; severity ranging from mild
incoordination, clumsiness to complete inability to walk, stand, or sit;
staggering, stumbling; loss of motor control |
Abnormal gait and posture, clumsiness and incoordination;
difficulties sitting, lying, crawling, and walking in infants and toddlers |
|
Toe walking |
Toe walking |
|
Difficulty in chewing or swallowing |
Difficulty chewing or swallowing |
|
Unusual postures |
Unusual postures |
|
Areflexia |
None described |
|
Tremors in general, tremors of the face and tongue, hand
tremors |
None described |
e. Cognition/Mental Function
Nearly all autistic individuals show impairment in some aspects of mental
function, even as other cognitive abilities remain intact. Most individuals may
test in the retarded range, while others have normal to above average IQs.
These characteristics are true in mercurialism. Moreover, the specific areas of
impairment are similar in the two disorders.
The impaired areas in autism are generally in (a) short term or working
memory and auditory and verbal memory; (b) concentration and attention,
particularly attention shifting; (c) visual motor and perceptual motor skills,
including eye-hand coordination; (d) language/verbal expression and
comprehension; and (e) using visually presented information when constraints
are placed on processing time. Relatively unimpaired areas include rote memory
skills, pattern recognition, matching, perceptual organization, and stimuli
discrimination. Higher level mental skills requiring complex processing are
typically deficient; these include (a) processing and filtering of multiple stimuli;
(b) following multiple step commands; (c) sequencing, planning and organizing;
and (d) abstract/conceptual thinking and symbolic understanding (Rumsey &
Hamburger, 1988; Plioplys, 1989; Bailey et al, 1996; Filipek et al, 1999;
Rumsey, 1985; Dawson, 1996; Schuler, 1995; Grandin, 1995; Sigman et al, 1987).
Younger or more mentally impaired children may have difficulties with symbolic
play and understanding object permanence or the mental state of others (Bailey
et al, 1996). Some autistic children are hyperlexic, showing superior decoding
skills while lacking comprehension of the words being read (Prizant, 1996). As
mentioned before, for most autistic individuals verbal IQ is lower than
performance IQ.
As in autism, Hg exposure causes some level of impairment primarily in (a)
short term memory and auditory and verbal memory; (b) concentration and
attention, including response inhibition; (c) visual motor and perceptual motor
skills, including eye-hand coordination; (d) language/verbal expression and
comprehension; and (e) simple reaction time. Hg-affected individuals may
present as "forgetful" or "confused." Performance IQ may be
higher than verbal IQ. "Degeneration of higher mental powers" has
resulted in (a) difficulty carrying out complex commands; (b) impairment in
abstract and symbolic thinking; and (c) deficits in constructional skills and
conceptual abstraction. One study mentions alexia, the inability to comprehend
the meaning of words, although reading of the words is intact (Yeates &
Mortensen, 1994; O'Carroll et al, 1995; Pierce et al, 1972; Snyder, 1972; Adams
et al, 1983; Kark et al, 1971; Amin-Zaki, 1974 and 1979; Davis et al, 1994;
Grandjean et al, 1997 & 1998; Myers & Davidson, 1998; Gilbert &
Grant-Webster 1995; Dales, 1972; Fagala and Wigg, 1992; Farnesworth, 1997;
Tuthill, 1899; Joselow et al, 1972; Rice, 1997; Piikivi et al, 1984; Vroom and
Greer, 1972). Even children exposed prenatally to "safe" levels of
methylmercury show lower scores on selective subtests of cognition, especially
in the domains of memory and attention, relative to unexposed controls
(Grandjean et al, 1998). In exposed juvenile monkeys, tests have revealed
delays in the development of object permanence, or the ability to conceptualize
the existence of a hidden object (Rice, 1996).
Research on mental retardation in autism is contradictory (Schuler, 1995).
The finding that "mental retardation or borderline intelligence often
co-exists with autism" (Filipek et al, 1999) is based on using standard
measures of intelligence (Gillberg & Coleman, 1992, p.32; Bryson, 1996);
other intelligence tests, designed to circumvent the language and attentional
deficits of autistic children, show significantly higher intelligence test
scores (Koegel et al, 1997; Russell et al, 1999). One study using such a
modified rating instrument has found 20% of autistic children to be mentally
retarded (Edelson et al, 1998), rather than the 70%-80% so scored on standard
tests. ASD individuals also show "strikingly uneven scores" on IQ
subtests, "unlike other disorders involving mental retardation, in which
subtest scores seem to be more or less even" (Bailey et al, 1996). Also
unlike typical cases of mental retardation, which is nearly always noted in the
peri- or neonatal periods, most parents of ASD children report infants of
seemingly normal appearance and development who were later characterized as
mentally retarded on tests. For example, one study compared early developmental
aberrations in mentally retarded children with and without autism. Findings indicated
that, whereas nearly all parents of the non-autistic mentally retarded study
group were aware of their child's impairment by age 3 months, nearly all
parents of the autistic children failed to notice any developmental
delays or issues until after 12 months of age (Baranek, 1999). Finally, there
are several case reports of autistic adults who were labeled mentally retarded
as children based on tests, who later "emerged" from their autism and
had normal IQs (ARI Newsletter, 1993, review).
As in autism, symptomatic mercury-poisoned victims can present with normal
IQs, borderline intelligence, or mental retardation; some may be so impaired as
to be untestable (Vroom and Greer, 1972; Davis et al, 1994). When lowered
intelligence is found, it is always reported as an obvious deterioration among
previously normally functioning people; this includes children exposed as
infants or toddlers (Dale, 1972; Vroom and Greer, 1972; Amin-Zaki, 1978). Once
the Hg-exposure source is removed, many (although not all) of these patients
"recover" their normal IQ, suggesting that "real" IQ was
not affected (Vroom and Greer, 1972; Davis et al, 1994). Infant monkeys given
low doses of Hg, while clearly impaired in visual, auditory, and sensory
functions, had intact central processing speed, which has been shown to
correlate with IQ in humans (Rice, 1997).
Table VI: Summary
of Areas of Mental Impairment
in Mercury Poisoning & Autism
|
Mercury
Poisoning |
Autism |
|
Some aspect of mental impairment in all symptomatic cases |
Some aspect of mental impairment in all cases |
|
Borderline intelligence on testing among previously normal
individuals; mental retardation occurring in severe cases of pre-/postnatal
exposure; some cases of MR reversible; primate studies indicate core intelligence
spared with low exposures |
Borderline intelligence or mental retardation on standard
tests among previously normally appearing infants; some cases of MR
"reversible"; indications that normal IQ might be present in
MR-labeled individuals |
|
Uneven performance on subtests of intelligence |
Uneven performance on subtests of intelligence |
|
Verbal IQ higher than performance IQ; compromised
language/verbal expression and comprehension |
Verbal IQ higher than performance IQ; compromised
language/verbal expression and comprehension |
|
Poor concentration, shortened attention span, general lack
of attention; poor response inhibition |
Lack of concentration, short attention span, lack of attention,
difficulty shifting attention |
|
Forgetfulness, loss of memory, particularly short term,
verbal and auditory memory; mental confusion |
Poor short term/working memory; poor auditory and verbal
memory; lower verbal encoding abilities |
|
Poor visual and perceptual motor skills, poor eye-hand
coordination; impairment in simple reaction time |
Poor visual and perceptual motor skills, poor eye-hand
coordination; lowered performance on timed tests |
|
Not reported as being tested |
Difficulty processing multiple stimuli |
|
Difficulty carrying out complex commands |
Difficulty carrying out multiple commands |
|
Alexia (inability to comprehend the meaning of written
words) |
Hyperlexia (ability to decode words while lacking word comprehension)
|
|
Deficits in constructional skills, conceptual abstraction,
understanding abstract ideas and symbolism; degeneration of higher mental
powers |
Deficits in abstract/conceptual thinking, symbolism,
understanding other's mental states; impairment in sequencing, planning,
organizing |
|
Lack of understanding of object permanence (primates) |
Deficient understanding of object permanence (children) |
f. Behaviors
Autism is associated with difficulties initiating and/or maintaining sleep;
hyperactivity and other ADHD traits; and self injurious behavior such as head
banging, even in the absence of mental retardation. Agitation, screaming,
crying, staring spells, stereotypical behaviors, and grimacing are common
(Gaedye, 1992; Gillberg and Coleman, 1992; Plioplys, 1989; Kanner, 1943;
Richdale, 1999; Stores & Wiggs, 1998). Kanner (1943) made a point of noting
excessive and open masturbation in two of the eleven young children comprising
his initial cases. Feeding and suckling problems are typical (Wing, 1980), and
restricted diets and narrow food preferences "are the rule rather than the
exception" (Gillberg and Coleman, 1992; Clark et al, 1993); some autistics
show a preference for salty foods (Shattock, 1997). Kanner, in his 1943
article, noted feeding problems from infancy, including vomiting and a refusal
to eat, in six of the eleven autistic children he described. There are case
studies of anorexia nervosa occurring in ASD patients, as well as an increased
likelihood of this eating disorder in families with ASD (Gillberg &
Coleman, 1992, p.99).
Humans and animals exposed to mercury develop unusual, abnormal, and
"inappropriate" behaviors (Florentine and Sanfilippo, 1991). Rats
exposed to mercury during gestation have exhibited stereotyped sniffing (Cuomo
et al, 1984) and hyperactivity (Fredriksson et al, 1996).
"Restlessness" has already been noted, and Davis et al (1994) found
poor response inhibition in their human subjects; both of these behaviors are closely
associated with ADHD in children. Babies and children with Hg poisoning exhibit
agitation, crying for no observable reason, grimacing, and insomnia (Pierce et
al, 1972; Snyder, 1972; Kark et al, 1971; Amin-Zaki, 1979; Florentine and
Sanfilippo, 1991; Aronow and Fleischmann, 1976). An 18 month old toddler with
otitis media, exposed to thimerosal in ear drops, had staring spells and
unprovoked screaming episodes (Rohyans et al, 1984). Symptoms of acrodynia in
babies and toddlers include continuous crying, anorexia and insomnia (Matheson
et al, 1980; Aronow and Fleischmann, 1976). These children were said to bang
their heads, have difficulty falling asleep, be irritable, and either refuse to
eat or only eat a few foods (Neville Recollection, Pink Disease Support Group
Site; Farnesworth, 1997). The frequent temper tantrums of a previously normal
12 year old, poisoned by mercury vapor, included hitting herself on the head
and screaming; furthermore, she had extreme genital burning and was observed to
masturbate even in front of others (Fagala and Wigg, 1992). Similarly,
priapism, persistent erection of the penis due to a pathologic condition
resulting in pain and tenderness, has been noted in boys with mercury poisoning
(Amin-Zaki et al, 1978).
Adults with mercury poisoning present with insomnia, agitation, and poor
appetite (Tuthill, 1899; Adams et al, 1983; Fagala and Wigg, 1992). Relative to
controls, more adults who had acrodynia in childhood have eating
idiosyncrasies, particularly a preference for salty foods to sweet ones
(Farnesworth, 1997), possibly because mercury causes excessive sodium
excretion, as shown in studies of dental amalgam placed in monkeys and sheep
(Lorscheider et al, 1995).
Table VII: Summary
of Unusual Behaviors
in Mercury-Poisoned Animals and Humans & in Autism
|
Mercury
Poisoning |
Autism |
|
Stereotyped sniffing (rats) |
Stereotyped, repetitive behaviors |
|
Hyperactivity (rats); poor response inhibition (humans),
restlessness |
Hyperactivity; ADHD-traits |
|
Agitation (humans) |
Agitation |
|
Insomnia; difficulty falling asleep (humans) |
Insomnia; difficulty falling or staying asleep |
|
Eating disorders: anorexia, poor appetite, food aversion,
narrow food preferences, decided food preferences (salty food) (humans) |
Eating disorders: anorexia; restricted diet/narrow food
preferences; feeding and suckling problems |
|
Masturbation, priapism (children) |
Masturbatory tendencies |
|
Unintelligible cries; continuous crying; unprovoked crying
(infants and children) |
Unprovoked crying |
|
Self injurious behavior, including head banging and
hitting the head (toddlers and children) |
Self injurious behavior, including head banging and
hitting the head |
|
Grimacing (children) |
Grimacing |
|
Staring spells (infants and children) |
Staring spells |
g. Vision
In autism, one of the earliest signs detected by mothers is a lack of eye
contact (Gillberg & Coleman, 1992), and an early diagnostic behavior is
failure to engage in joint attention based on the ability to "look where
you are pointing" (CHAT, Baron-Cohen et al, 1992). Of 11 autistic children
studied, ten had inaccurate or slow visual saccades (Rosenhall et al, 1988).
Although some adults with ASD report exceptional visual acuity, visual problems
are common, with two separate studies reporting 50% of ASD subjects having some
type of unusual visual impairment (Steffenburg, in Gillberg & Coleman,
1992). Ritvo et al (1986) and Creel et al (1989) found decreased function of
the rods in a study of autistic people, including a retinal sheen, and noted
that many such individuals tend to use peripheral vision because of this. A
number of case reports describe over-sensitivity to light and blurred vision
(Sperry, 1998; Gillberg & Coleman, 1992, p.29; O'Neill & Jones, 1997).
Mercury can lead to a variety of vision problems, especially in children
(Pierce et al, 1972; Snyder, 1972). Children who ate high doses of mercury from
contaminated pork developed blindness (Snyder, 1972). In Iraqi babies exposed
prenatally there was blindness or impaired vision (Amin-Zaki, 1974 and 1979).
Iraqi children exposed postnatally developed visual disturbances, which ranged
from blurred or hazy vision to constriction of the visual fields to complete
blindness (Amin-Zaki et al, 1978). Two girls with mercury vapor poisoning were
found to have visual field defects (Snyder, 1972), and, as previously noted,
one child with Hg poisoning developed gaze avoidance (Fagala & Wigg, 1992).
Acrodynia sufferers report vision problems, including near-sightedness and
light sensitivity or photophobia (Diner and Brenner, 1998; Neville
Recollection, Pink Disease site; Farnesworth, 1997; Matheson et al, 1980;
Aronow and Fleischmann, 1976). A 25 year old man with elemental mercury
poisoning exhibited decreased visual acuity, difficulty with visual fixation,
and constricted visual fields (Kark et al, 1971). In Japanese victims, there
was blurred vision as well as constriction of visual fields (Snyder, 1972;
Tokuomi et al, 1982). Iraqi mothers exposed to Hg had visual disturbance
(Amin-Zaki, 1979).
In dogs exposed to daily doses of methylmercury, distortion of the visual
evoked response from the visual cortex was the first sign. Damage occurred in
the preclinical silent stage, demonstrating that CNS damage is occurring before
overt symptoms appear (Mattsson et al, 1981). Monkeys treated at birth with low
level methylmercury exhibited impaired spatial vision and visual acuity at age
3 and 4 years (Rice and Gilbert, 1982). Disturbances caused by methylmercury in
rat optic nerves were observed (Kinoshita et al, 1999).
Table VIII:
Summary of Visual Impairments
Seen in Mercury Poisoning & Autism
|
Mercury
Poisoning |
Autism |
|
Lack of eye contact; difficulties with visual fixation |
Lack of eye contact; gaze abnormalities; problems in joint
attention |
|
"Visual impairments," blindness,
near-sightedness, decreased visual acuity |
"Visual impairments"; inaccurate or slow saccades;
decreased functioning of the rods; retinal sheen |
|
Light sensitivity, photophobia |
Over-sensitivity to light |
|
Blurred or hazy vision |
Blurred vision |
|
Constricted visual fields |
Not described |
h. Physical Presentations
There is a much higher rate of autism among children with cerebral palsy than
would be expected by chance (Nordin and Gillberg, 1996). Many autistic children
have abnormal muscle tone including hyper- and hypotonia, and many are
incontinent or have difficulty being toilet trained (Filipek et al, 1999;
Church and Coplan, 1995). Several of the infants which Teitelbaum and
colleagues (1998) observed showed decreased arm strength, and Schuler (1995)
describes greater muscle weakness in the upper than the lower body. Impairments
in oral-motor function, including problems chewing and swallowing, are common,
as noted previously.
These impairments are seen in mercurialism as well. In the Iraqi and
Japanese epidemics, many children developed clinical cerebral palsy (Amin-Zaki,
1979; Myers & Davidson, 1998; Gilbert & Grant-Webster 1995; Dale,
1972). Amin-Zaki et al (1978) reported muscle wasting and lack of motor power
and control in most cases, complete paralysis in several cases, and athetotic
movements in 2 cases, of postnatally exposed children. In the Iraqi babies and
children, some had increased muscle tone, while others had decreased muscle
tone. Abnormal reflexes, spasticity, and weakness were common. One child said
"my hands are weak and do not obey me" (Amin-Zaki et al, 1974 and
1978). The 12 year old who inhaled mercury vapor exhibited weakness and
decreased muscle strength (Fagala and Wigg, 1992). As in autism, muscle
weakness from mercury poisoning is most prominent in the upper body (Adams et
al, 1983). Acrodynia, for example, is marked by poor muscle tone in general and
loss of arm strength in particular (Farnesworth, 1997). Finally, difficulty in
chewing and swallowing, salivation, and drooling are common in children as well
as adults; incontinence was observed in children in the Iraqi Hg-crisis
(Amin-Zaki, 1974 and 1978; Pierce et al, 1972; Snyder, 1972; Joselow et al,
1972; Smith, 1977).
The presence of rashes and dermatitis is sometimes reported in descriptions
of ASD subjects. Whiteley et al (1998) found that 63% of the ASD children had a
history of eczema or other skin complaints. "Some children with autism are
frequent scratchers. Gentle rubbing and scratching can become a calming
self-stimulation; but when it becomes clawing, and there are rashes and open
scrapes on the skin, a tactile intolerance can be responsible" (O'Neill,
1999).
Rashes and itching are common disturbances in mercury toxicity as well (Kark
et al, 1971). A 4 year old with Hg poisoning developed an itchy, peeling rash
on the extremities (Florentine and Sanfilippo, 1991). Mercury vapor inhalation
caused a rash and peeling on the palms and soles of a pre-adolescent (Fagala
and Wigg, 1992). An acrodynia victim described himself as a child as having
severe itching and a constant burning sensation at the extremities, resulting
in him rubbing his hands and feet raw (Neville Recollection, Pink Disease
Support Group). Acrodynia symptoms in an adult poisoned by ethylmercury
injection included pink scaling palms and soles, flushed cheeks, and itching
(Matheson et al, 1980). In acrodynia the skin may be rough and dry, and the
soles and palms are usually but not necessarily red (Aronow and Fleischmann,
1976). Thimerosal ingested by 44 year old man led to dermatitis (Pfab et al,
1996).
In autism, "signs of autonomic disturbance may be noticed at times,
including sweating, irregular breathing, and rapid pulse" (Wing and
Attwood, 1987). There may be elevated blood flow and heart rate (Ornitz, 1987).
An increased incidence of acrocyanosis has been observed in Asperger's
syndrome. Acrocyanosis is an uncommon disorder of poor circulation in which
skin on the hands and feet turn red and blue; there is profuse sweating; and
the fingers and toes are persistently cold (Carpenter and Morris, 1991).
Sweating and circulatory abnormalities are also common in some forms of
mercury poisoning. Acrodynia in adults and children results in excessive
sweating, poor circulation, and rapid heart rate (Farnesworth, 1997; Matheson
et al, 1980; Cloarec et al, 1995; Warkany and Hubbard, 1953). The 12 year old
with mercury vapor poisoning sweated profusely, especially at night (Fagala and
Wigg, 1992), and elevated blood pressure has been reported in exposed workers
(Vroom and Greer, 1972). Autonomic system abnormalities can be caused by
disturbances in acetylcholine levels, known to be deficient in both autism and
Hg poisoning (see neurotransmitter section below).
Table IX: Physical
Disturbances
in Mercury Poisoning & Autism
|
Mercury
Poisoning |
Autism |
|
Increase in cerebral palsy; hyper- or hypotonia;
paralysis, abnormal reflexes; spasticity; decreased muscle strength and motor
power, especially in the upper body; incontinence; problems chewing,
swallowing, and salivating |
Increase in cerebral palsy; hyper- or hypotonia; decreased
muscle strength, especially in the upper body; incontinence/toilet training
difficulties; problems chewing and swallowing |
|
Rashes, dermatitis, dry skin, itching; burning sensation |
Rashes, dermatitis, eczema; itching |
|
Autonomic disturbances: excessive sweating; poor
circulation; elevated heart rate |
Autonomic disturbances: sweating abnormalities; poor
circulation; elevated heart rate |
j. Gastrointestinal Function
Many if not most autistic individuals have gastrointestinal problems, the most
common complaints being chronic diarrhea, constipation, gaseousness, and
abdominal discomfort and distention (D'Eufemia et al, 1996; Horvath et al,
1999; Whitely et al, 1998). Colitis is not uncommon (Wakefield et al, 1998). As
noted previously, anorexia is sometimes associated with ASD (Gillberg &
Coleman, 1992). Kanner noted that over half his initial cases had feeding
difficulties and excessive vomiting as infants (1943). O'Reilly and Waring
(1993) have described sulfur deficiencies in autism, an effect of which can be
clumping of proteins on the gut wall, which is lined with sulfated proteins.
The clumping can lead to increased intestinal permeability, or leaky gut
syndrome (Shattock, 1997), found in many autistic individuals (D'Eufemia,
1996). Some ASD individuals have unusual opioid peptide fragments in urine;
these peptides are believed to enter the bloodstream due to a leaky gut and to
result from an incomplete breakdown of gluten and casein in the diet possibly
arising from "inadequacy of the [endopeptidase] enzyme systems which are
responsible for their breakdown" (Shattock, 1997).
Mercury, which binds to sulfur groups (Clarkson, 1992), is known to cause gastroenteritis (Kark et al, 1971). For example, a four year old with diarrhea was initially diagnosed with gastroenteritis (Florentine and Sanfilippo, 1991). A pre-adolescent with mercury vapor poisoning developed nausea, abdominal pain, poor appetite, rectal itching, and diarrhea; she frequently strained to have a bowel movement, and was at one point diagnosed with colitis (Fagala and Wigg, 1992). Acrodynia is marked by both constipation and diarrhea (Diner and Brenner, 1998). Incontinence of urine and stool are observed in infants and children exposed pre- and postnatally in Iraq (Amin-Zaki, 1974 and 1978). In another case, a 28 year old woman with occupational exposure to mercury vapor developed watery stools (Ross et al, 1977). Diarrhea and digestive disturbance were seen in a dentist with measurable mercury levels; there was obesity in another dentist (Smith, 1977). A 44 year old man poisoned with thimerosal given intramuscularly developed gastrointestinal bleeding, whi