Rapid-onset dystonia-parkinsonism

Howard L. Geyer, Susan B. Bressman

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

Rapid-onset dystonia-parkinsonism (RDP) is a rare condition with autosomal-dominant inheritance causing dystonia and parkinsonism which develop over a short period of time. It results from abnormalities in the Na+/K+-ATPase pump due to mutations in the ATP1A3 gene. This chapter reviews the clinical features, genetics, and diagnosis of this disorder.

Original languageEnglish (US)
Pages (from-to)559-562
Number of pages4
JournalHandbook of Clinical Neurology
Volume100
DOIs
StatePublished - Apr 20 2011

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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