Unusual compulsive motor activity during treatment with clothiapine in a mentally retarded adolescent

Brain Dev. 2004 Sep;26(6):409-11. doi: 10.1016/j.braindev.2003.11.008.

Abstract

Atypical antipsychotic agents, specifically those with a high hyposerotonergic activity such as clozapine and clothiapine, have been associated with de novo obsessive-compulsive symptoms. We report the case of a 16-year-old adolescent male with severe mental impairment and disruptive behaviour who developed a compulsive head and body turning disorder on clothiapine. Such a symptom had to be distinguished from epileptic partial seizures; it promptly disappeared with the drug discontinuation.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Antipsychotic Agents / adverse effects
  • Attention Deficit and Disruptive Behavior Disorders / drug therapy*
  • Attention Deficit and Disruptive Behavior Disorders / etiology
  • Compulsive Behavior / chemically induced*
  • Compulsive Behavior / physiopathology
  • Diagnosis, Differential
  • Dibenzothiazepines / adverse effects*
  • Dose-Response Relationship, Drug
  • Dyskinesia, Drug-Induced / physiopathology*
  • Epilepsy, Partial, Motor / diagnosis
  • Haloperidol / therapeutic use
  • Humans
  • Hyperkinesis / chemically induced*
  • Hyperkinesis / physiopathology
  • Intellectual Disability / complications*
  • Intellectual Disability / psychology
  • Male

Substances

  • Antipsychotic Agents
  • Dibenzothiazepines
  • Haloperidol
  • clothiapine