http://neurology.medscape.com/reuters/prof/2001/08/08.07/20010806scie003.html
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LONDON (Reuters Health) Aug 06 - Scientists at
Oxford University said on Monday that they are zeroing in on genes that might
make children susceptible to developing autism. Their discovery that sections of certain chromosomes are linked to the
disorder helps confirm other research showing there is an inherited component
to the condition. Pinpointing the genes involved could help doctors develop
treatments for the baffling condition, which strikes at least 5 in 10,000
children within the first 3 years of life. "Currently there is no consensus amongst researchers about what is
actually going wrong in the brain when a child develops autism," said
Professor Anthony Monaco, director of the Wellcome Trust Centre for Human
Genetics at Oxford. However, "the discovery of these regions...confirms
the genetic component of autism and will enable us to narrow our search down
to specific genes and the functions they control. This should cast light on
what is going wrong, and hopefully give us clues on how autism could be
treated." The scientists, who are part of the International Molecular Genetic Study
of Autism Consortium, screened the genomes of over 150 pairs of siblings with
autism. They found two regions on chromosomes 2 and 17 that may house genes
responsible for susceptibility to the disease. In addition, their study shored up previous findings that areas on
chromosomes 7 and 16 are also significant in determining if an individual is
likely to develop autism. Members of the international research team, which includes scientists from
Europe and the US, are now planning to extend their work to identify the
specific genes responsible for the condition, Monaco told Reuters Health.
These genes are believed to play a key role in brain development and
signalling. Monaco said the international study would focus on identifying those genes
that show signs of mutation. "Gene mutations show susceptibility to
disease and that is what we are looking for in this study. Why we have
mutations, we are presently unable to say."
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