1% Of Autism Due To Unstable Genes
Specific Genetic Instability Causes 1 In 100 Autism Cases
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Play CBS Video Video Gene Defect Linked To Autism Researchers have discovered a genetic defect that can increase the risk of autism by as much as 100 times. Susan McGinnis reports.
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Video HealthWatch Meg Oliver reports on gene research that can help detect autism; teen abuse of cough medicine to get high; and looking for a genetic link for drug abuse.
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Video A Genetic Link To Autism A new study links autism to genetic defects. CBS News Medical Correspondent Dr. Jon LaPook reports.
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(CBS/AP)
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Interactive Breaking The Silence Find out more about autism, and where to get help for someone who may have this neurological disorder.
The genes are located on an arm of the human chromosome that's still young in terms of evolution. This means it carries highly similar stretches of genetic code that cross over in the earliest stages of embryo development. This crossover means that genes in the segment can be cut out (deleted) or copied too many times (duplicated).
Deletion or duplication of genes in this region "carries substantial susceptibility to autism and appear to account for approximately 1% of cases," report Massachusetts General Hospital researchers Lauren A. Weiss, PhD, Mark J. Daly, PhD, and colleagues.
This is at least as large a subset of autism cases as any other single factor is known to cause, the researchers note. A duplicated gene in another chromosome causes the Prader-Willi and Angelman autism syndromes, which account for about 1% of autism cases.
So far, researchers believe about 10% of autism cases have genetic causes. Many of these genetic abnormalities cause other profound disabilities in addition to autism.
The newly discovered abnormality, at a chromosomal site called 16p11.2, appears to cause early-onset autism. Developmental regression - in which apparently normal, usually 14- to 24-month old children seem to backslide into autism - was not seen in children with the 16p11.2 abnormality.
Weiss and colleagues found the 16p11.2 abnormality using sophisticated genetic techniques to search the genomes of 751 families with two or more cases of autism. The abnormality was seen only in people with autism.
Because it is caused by a misreading of the genetic code, the genetic abnormality is not directly inherited from parents. Many cases of autism may result from various rare genetic deletions or duplications. This could be why it's been so hard to identify specific "autism genes."
On the other hand, researchers now see autism as a collection of many different syndromes - and even within these syndromes there may be very different autistic symptoms . As we learn more and more about autism, it's like peeling back the layers of an onion, suggest Evan E. Eichler, PhD, and Andrew W. Zimmerman, MD, in an editorial accompanying the Weiss report.
They suggest that larger studies, using the new techniques pioneered by Weiss and colleagues, "may be needed to peel away the remaining layers of the onion."
The Weiss study, and the Eichler/Zimmerman editorial, appear ahead of print in the Jan. 9 Online First issue of The New England Journal of Medicine.
By Daniel DeNoon
Reviewed by Louise Chang
©2008 WebMD, Inc. All rights reserved.
- And for the other 99%?
Posted by brianbwb
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Piffle. The other 99% probably ate the imported Dora toys coated with lead and/or date rape drug. :-o - Reply to this comment
- And for the other 99%?
- Reply to this comment
- Well this convinces me that vaccines laced with mercury are not responsible. More disinformation from Big Pharma''s propaganda unit Web MD.
- Reply to this comment
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