Prader-Willi syndrome and psychotic symptoms: 1. Case descriptions and genetic studies

J Intellect Disabil Res. 1998 Dec:42 ( Pt 6):440-50. doi: 10.1046/j.1365-2788.1998.4260440.x.

Abstract

Six people with Prader-Willi syndrome (PWS) who developed psychoses are described. Along with other literature reviewed in the present paper, the results imply an association between PWS and psychotic symptoms. Genetic studies were possible in five cases and SNRPN expression was examined in three cases. Maternal uniparental disomy and 15q11q13 deletions were found, demonstrating that psychotic symptoms are not associated with a single type of genetic abnormality.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Chromosome Deletion
  • Chromosomes, Human, Pair 16 / genetics
  • Female
  • Humans
  • Male
  • Prader-Willi Syndrome / genetics*
  • Prader-Willi Syndrome / psychology*
  • Psychotic Disorders / diagnosis*
  • Psychotic Disorders / psychology*
  • X Chromosome / genetics