Rapid-onset dystonia-parkinsonism

Howard Geyer, Susan B. Bressman

Research output: Book/ReportBook

4 Citations (Scopus)

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)
PublisherUnknown Publisher
Number of pages4
Volume100
DOIs
StatePublished - 2011

Publication series

NameHandbook of Clinical Neurology
Volume100
ISSN (Print)00729752

Fingerprint

Inborn Genetic Diseases
Dystonia
Parkinsonian Disorders
Mutation
Genes
Dystonia 12
sodium-translocating ATPase

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Geyer, H., & Bressman, S. B. (2011). Rapid-onset dystonia-parkinsonism. (Handbook of Clinical Neurology; Vol. 100). Unknown Publisher. https://doi.org/10.1016/B978-0-444-52014-2.00040-9

Rapid-onset dystonia-parkinsonism. / Geyer, Howard; Bressman, Susan B.

Unknown Publisher, 2011. 4 p. (Handbook of Clinical Neurology; Vol. 100).

Research output: Book/ReportBook

Geyer, H & Bressman, SB 2011, Rapid-onset dystonia-parkinsonism. Handbook of Clinical Neurology, vol. 100, vol. 100, Unknown Publisher. https://doi.org/10.1016/B978-0-444-52014-2.00040-9
Geyer H, Bressman SB. Rapid-onset dystonia-parkinsonism. Unknown Publisher, 2011. 4 p. (Handbook of Clinical Neurology). https://doi.org/10.1016/B978-0-444-52014-2.00040-9
Geyer, Howard ; Bressman, Susan B. / Rapid-onset dystonia-parkinsonism. Unknown Publisher, 2011. 4 p. (Handbook of Clinical Neurology).
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