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Dystonia in Parkinson's disease: clinical and pharmacological features.

Abstract
We studied the features of dystonia in 9 patients with untreated idiopathic Parkinson's disease and in 56 patients on sustained treatment with L-dopa. Dystonia was seen as an initial symptom in patients with both early- and late-onset Parkinson's disease and included action dystonia of the limbs and cranial dystonia. Although the coexistence of parkinsonism and dystonia suggests a common pathophysiology, antiparkinsonian drugs did not consistently influence dystonic spasms. L-dopa-induced dystonia was seen as an off-period, biphasic, or peak-dose phenomenon. Each type showed a distinctive pattern of localization of dystonic spasms, possibly reflecting neurochemical aspects of basal ganglia somatotopy. Neuropharmacological studies performed in 12 patients suggest that off-period dystonia is genuinely induced by L-dopa and best relieved by antiparkinsonian agents.
AuthorsW H Poewe, A J Lees, G M Stern
JournalAnnals of neurology (Ann Neurol) Vol. 23 Issue 1 Pg. 73-8 (Jan 1988) ISSN: 0364-5134 [Print] United States
PMID3345068 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Levodopa
Topics
  • Adult
  • Aged
  • Circadian Rhythm
  • Dose-Response Relationship, Drug
  • Dystonia (chemically induced, drug therapy, etiology, physiopathology)
  • Humans
  • Injections, Intravenous
  • Levodopa (adverse effects)
  • Middle Aged
  • Parkinson Disease (complications, drug therapy)
  • Substance Withdrawal Syndrome (physiopathology)

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