The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

Neurobiology of Disease
Amber HogartN Carolyn Schanen

Abstract

A cluster of low copy repeats on the proximal long arm of chromosome 15 mediates various forms of stereotyped deletions and duplication events that cause a group of neurodevelopmental disorders that are associated with autism or autism spectrum disorders (ASD). The region is subject to genomic imprinting and the behavioral phenotypes associated with the chromosome 15q11.2-q13 disorders show a parent-of-origin specific effect that suggests that an increased copy number of maternally derived alleles contributes to autism susceptibility. Notably, nonimprinted, biallelically expressed genes within the interval also have been shown to be misexpressed in brains of patients with chromosome 15q11.2-q13 genomic disorders, indicating that they also likely play a role in the phenotypic outcome. This review provides an overview of the phenotypes of these disorders and their relationships with ASD and outlines the regional genes that may contribute to the autism susceptibility imparted by copy number variation of the region.

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Related Concepts

Autistic Disorder
Autosome Abnormalities
Chromosomes, Human, Pair 15
Royer Syndrome
Angelman Syndrome
Alleles
Autistic Disorder
Brain
Genes
Stereotypic Movement Disorder

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