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Suppression of myoclonus in SCA2 by piracetam.

Abstract
We report on a 30-year-old patient with advanced cerebellar degeneration due to SCA2. He presented with severe myoclonus, which was resistant to conventional therapy and dramatically improved after administration of 12-18 gm/die piracetam. Piracetam may be considered in the treatment of refractory myoclonus in spinocerebellar degenerations.
AuthorsAnna De Rosa, Pasquale Striano, Fabrizio Barbieri, Arturo de Falco, Carlo Rinaldi, Tecla Tucci, Salvatore Striano, Alessandro Filla, Giuseppe De Michele
JournalMovement disorders : official journal of the Movement Disorder Society (Mov Disord) Vol. 21 Issue 1 Pg. 116-8 (Jan 2006) ISSN: 0885-3185 [Print] United States
PMID16149096 (Publication Type: Case Reports, Journal Article)
CopyrightCopyright (c) 2005 Movement Disorder Society.
Chemical References
  • Ataxins
  • Nerve Tissue Proteins
  • Piracetam
Topics
  • Adult
  • Ataxia (drug therapy, genetics)
  • Ataxins
  • Dose-Response Relationship, Drug
  • Gait Ataxia (drug therapy, genetics)
  • Humans
  • Infusions, Intravenous
  • Male
  • Myoclonus (drug therapy, genetics)
  • Nerve Tissue Proteins (genetics)
  • Neurologic Examination (drug effects)
  • Piracetam (adverse effects, therapeutic use)
  • Recurrence
  • Spinocerebellar Ataxias (drug therapy, genetics)
  • Substance Withdrawal Syndrome (diagnosis)
  • Treatment Outcome
  • Trinucleotide Repeats (genetics)

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