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Haloperidol-Induced Tardive Dyskinesia in a Child With Gilles de la Tourette's Disease
Eli M. Mizrahi, MD;
David Holtzman, MD, PhD;
Barry Tharp, MD
Arch Neurol. 1980;37(12):780.
Abstract
A 7-year-old boy with multiple tic or Gilles de la Tourette's disease was treated with haloperidol. Within five months, lingual-buccal-facial movements developed that were characteristic of tardive dyskinesia. This new movement disorder disappeared after treatment with haloperidol was stopped. To our knowledge, this is the first report of tardive dyskinesia complicating the use of haloperidol in the treatment of multiple tic syndrome in a child.
Author Affiliations
From the Departments of Neurology and Pediatrics, Stanford (Calif) University School of Medicine.
Footnotes
Accepted for publication March 27, 1980.
Reprint requests to Division of Pediatric Neurology, Stanford University School of Medicine, Stanford, CA 94305 (Dr Holtzman).
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