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Tardive dyskinesia in Tourette syndrome.

Abstract
Three patients are reported who developed oral-buccal-lingual movements typical of tardive dyskinesia while being treated with stable doses of haloperidol for Tourette syndrome. In each case signs resolved within a number of weeks after medication was discontinued. One of the patients experienced recurrence of the dyskinesia during a challenge with phenothiazine tranquilizers. In each case the dose of haloperidol was well within the usual therapeutic range. A strong family history of movement disorders, including Tourette syndrome, was present in each family.
AuthorsG S Golden
JournalPediatric neurology (Pediatr Neurol) 1985 May-Jun Vol. 1 Issue 3 Pg. 192-4 ISSN: 0887-8994 [Print] United States
PMID3880404 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Haloperidol
Topics
  • Adolescent
  • Adult
  • Dyskinesia, Drug-Induced (etiology)
  • Female
  • Haloperidol (adverse effects, therapeutic use)
  • Humans
  • Male
  • Tourette Syndrome (drug therapy, genetics)

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