Recurrent brief depression in Prader-Willi syndrome: a case report

Psychiatr Genet. 1997 Spring;7(1):41-4. doi: 10.1097/00041444-199700710-00007.

Abstract

Prader-Willi syndrome is caused by a deletion of 15q11-13 or maternal disomy of chromosome 15. A female patient with Prader-Willi syndrome, who was 19 years of age at the first onset of her recurrent brief episodes, is described. The episodes showed a near-monthly rhythm and were followed by a spontaneous remission in 7-18 days. The symptoms during the episodes were anorexia, insomnia, guilt feelings, ideas of being doomed, ostracized and persecuted, and stupor alternating with agitation.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Antidepressive Agents / therapeutic use
  • Chromosome Deletion
  • Chromosomes, Human, Pair 15 / genetics
  • Depressive Disorder / complications*
  • Depressive Disorder / drug therapy
  • Depressive Disorder / genetics
  • Female
  • Humans
  • Lithium / therapeutic use
  • Prader-Willi Syndrome / complications
  • Prader-Willi Syndrome / genetics
  • Prader-Willi Syndrome / psychology*
  • Recurrence

Substances

  • Antidepressive Agents
  • Lithium