Obsessive-compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene

Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):361-4. doi: 10.1002/ajmg.b.30431.

Abstract

Prior studies suggest that obsessive-compulsive symptoms (OCS) and disorder (OCD) are co-morbid with dystonia. We tested if OCS/OCD is a clinical manifestation of the DYT1 dystonia mutation by interviewing members of families with an identified DYT1 mutation, and classifying by manifesting carriers (MC), non-manifesting carriers (NMC), and non-carriers (NC). We found that OCD/OCS are not increased in DYT1 mutation carriers compared with NC, nor is OCD associated with manifesting DYT1 dystonia.

Publication types

  • Multicenter Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Dystonia / genetics
  • Female
  • Heterozygote
  • Humans
  • Male
  • Middle Aged
  • Molecular Chaperones / genetics*
  • Mutation
  • Obsessive-Compulsive Disorder / genetics*
  • Phenotype

Substances

  • Molecular Chaperones
  • TOR1A protein, human