DISC1 duplication in two brothers with autism and mild mental retardation

Clin Genet. 2010 Apr;77(4):389-94. doi: 10.1111/j.1399-0004.2009.01318.x. Epub 2009 Dec 10.


We describe the identification and delineation of an inherited 2.07 Mb microduplication in 1q42.2 in two brothers with autism and mild mental retardation. Since this duplication was not present in 1577 Belgian persons, we consider this as an extremely rare variant which has the potential to provide further insight into the genetics of autism. The duplication contains seven genes including the DISC1 gene, an interesting candidate gene that has been associated to schizophrenia, bipolar disorder, autism and Asperger syndrome. In this report we describe additional analyses undertaken to investigate the causal relationship of the duplication to the autism phenotype. We conclude that the 1q42.2 microduplication probably confers susceptibility to autism in the current family. This study is a typical illustration of the difficult interpretation of causality of a very rare variant in neuropsychiatric disease and the challenge of genetic counselling in a particular family.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autistic Disorder / complications*
  • Autistic Disorder / genetics*
  • Child
  • Child, Preschool
  • Chromosome Aberrations
  • Chromosomes, Human, Pair 1 / genetics
  • Family
  • Female
  • Gene Duplication*
  • Humans
  • Infant, Newborn
  • Intellectual Disability / complications*
  • Intellectual Disability / genetics*
  • Male
  • Nerve Tissue Proteins / genetics*
  • Pedigree
  • Pregnancy
  • Siblings*


  • DISC1 protein, human
  • Nerve Tissue Proteins