Rapid-onset dystonia-parkinsonism

Howard L. Geyer; Susan B. Bressman

doi:10.1016/B978-0-444-52014-2.00040-9

Rapid-onset dystonia-parkinsonism

Howard L. Geyer, Susan B. Bressman

Neurology

Research output: Contribution to journal › Article › peer-review

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 language	English (US)
Pages (from-to)	559-562
Number of pages	4
Journal	Handbook of Clinical Neurology
Volume	100
DOIs	https://doi.org/10.1016/B978-0-444-52014-2.00040-9
State	Published - 2011

ASJC Scopus subject areas

Neurology
Clinical Neurology

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10.1016/B978-0-444-52014-2.00040-9

Cite this

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title = "Rapid-onset dystonia-parkinsonism",

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.",

author = "Geyer, {Howard L.} and Bressman, {Susan B.}",

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AU - Geyer, Howard L.

AU - Bressman, Susan B.

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N2 - 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.

AB - 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.

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SP - 559

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JO - Handbook of Clinical Neurology

JF - Handbook of Clinical Neurology

ER -

Rapid-onset dystonia-parkinsonism

Abstract

ASJC Scopus subject areas

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