Variable phenotype of rapid-onset dystonia-parkinsonism

A. Brashear, M. R. Farlow, I. J. Butler, E. J. Kasarskis, W. B. Dobyns

Research output: Contribution to journalArticle

46 Scopus citations

Abstract

Rapid-onset dystonia-parkinsonism (RDP) is an autosomal dominant disorder characterized by the rapid onset of dystonic spasms and parkinsonism over a period of a few hours to weeks after their onset. We have seen two additional members of this previously reported family with RDP who present with a more gradual progression of their disorder over 6-18 months. One of these individuals experienced the rapid progression of symptoms 2 years after an initial stabilization of his condition. The RDP phenotype is variable, and presentation may be gradual in some cases. Cerebrospinal fluid neurotransmitter levels in these two and other family members suggest involvement of the dopaminergic pathways in RDP.

Original languageEnglish (US)
Pages (from-to)151-156
Number of pages6
JournalMovement Disorders
Volume11
Issue number2
DOIs
StatePublished - Mar 25 1996
Externally publishedYes

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Keywords

  • Dopamine
  • Dystonia
  • Homovanillic acid
  • Parkinsonism
  • Parkinsonism
  • Rapid-onset dystonia

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Cite this

Brashear, A., Farlow, M. R., Butler, I. J., Kasarskis, E. J., & Dobyns, W. B. (1996). Variable phenotype of rapid-onset dystonia-parkinsonism. Movement Disorders, 11(2), 151-156. https://doi.org/10.1002/mds.870110206