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

Amber Hogart, David Wu, Janine M LaSalle, N. Carolyn Schanen

Research output: Contribution to journalArticle

175 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)181-191
Number of pages11
JournalNeurobiology of Disease
Volume38
Issue number2
DOIs
StatePublished - May 2010
Externally publishedYes

Keywords

  • Angelman syndrome
  • Autism
  • Autism spectrum disorders
  • Imprinting
  • Interstitial duplication chromosome 15
  • Isodicentric chromosome 15
  • Low copy repeats
  • Prader-Willi syndrome

ASJC Scopus subject areas

  • Neurology

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