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Abstract | Summary
| Original Article
Mapping the genes for autism:
Canadian
study
part of a worldwide effort
Is autism a genetically inherited disorder? If so, which gene or
genes are responsible?
More than 170 of the world’s leading
genetic researchers, including about a dozen right here in Canada,
are searching for
the answers by going to the most likely source, families who have
two or more children affected with the disorder.
More than 1,200
families from all over the world, including 200 families across
Canada, are participating in this global research
collaboration, the largest ever assembled to locate the genes
associated with autism spectrum disorders. The Canadian study is
funded by
the Canadian Institutes for Health Research. The project involves
collecting blood and DNA samples from parents and their children
to track inheritance in families and to better understand the
genetic-biochemical changes causing autism and Pervasive Developmental
Disorder (PDD).
The Canadian study is being led by Peter Szatmari of the
Offord
Centre for Child Studies in Hamilton, Ontario, and Steve Scherer
of The Hospital for Sick Children in Toronto. The group is
looking for two types of genes: susceptibility genes, which are
responsible for the inherited risk for autism; and modifier genes,
which are not directly responsible for autism but which may have
an
effect
on clinical expression and could help to shed light on why
symptoms can vary so greatly from one individual to another.
Locating
the genes will be no easy task. There are approximately
30,000 genes in the 23 chromosomes that make up the human
genome. Roughly 4,000 of these genes are located in the brain.
Autism is known as a complex disorder that is believed to involve
many genes
on several chromosomes.
Preliminary findings have zeroed in
on Chromosome 7 as one hot spot for continued research. But while
results are promising,
there remains much work to be done. Researchers hope eventually
to enable
clinicians to biologically diagnose autism, allowing children
to be diagnosed earlier than ever and leading to more effective
treatments
and better outcomes for them and their families. Knowing
what causes autism may even allow us, one day, to prevent
it.
Researchers involved in the Canadian study include:
Susan Bryson, PhD,
Dalhousie University
Jeremy Goldberg, MD, McMaster University
Marshall Jones, PhD, The Pennsylvania State University,
College of Medicine
Bill Mahoney, MD, McMaster University
Chantal Merette, PhD, Laval University
Roberta Palmour, MD, McGill University
Andrew Paterson, MD, University of Toronto
Wendy Roberts, MD, University of Toronto
Lawrence Tuff, PhD, McMaster University
John Vincent, PhD, University of Toronto
Lonnie Zwaigenbaum, MD, McMaster University.
Participate in this
study
Learn more about this global genetics study
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