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Dramatic levodopa responsiveness of dystonia in a sporadic case of spinocerebellar ataxia type 3.

Abstract
A genetically confirmed case of spinocerebellar ataxia type 3 (SCA 3), presenting with disabling foot dystonia, peripheral neuropathy, and minimal cerebellar signs is reported. The dystonia improved dramatically with levodopa treatment in the absence of additional parkinsonian feature. A trial of levodopa for dystonia in SCA 3 may be of therapeutic benefit, at least in the initial stage of the disease.
AuthorsR Nandagopal, S G K Moorthy
JournalPostgraduate medical journal (Postgrad Med J) Vol. 80 Issue 944 Pg. 363-5 (Jun 2004) ISSN: 0032-5473 [Print] England
PMID15192175 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Antiparkinson Agents
  • Levodopa
Topics
  • Adult
  • Antiparkinson Agents (therapeutic use)
  • Dystonic Disorders (drug therapy)
  • Humans
  • Levodopa (therapeutic use)
  • Machado-Joseph Disease (diagnosis, drug therapy)
  • Magnetic Resonance Imaging
  • Male

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