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

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

7 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
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
Externally published	Yes

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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.\}",

year = "2011",

doi = "10.1016/B978-0-444-52014-2.00040-9",

language = "English",

volume = "100",

pages = "559--562",

journal = "Handbook of Clinical Neurology",

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publisher = "Elsevier B.V.",

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T1 - Rapid-onset dystonia-parkinsonism

AU - Geyer, Howard L.

AU - Bressman, Susan B.

PY - 2011

Y1 - 2011

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.

UR - https://www.scopus.com/pages/publications/79954520051

U2 - 10.1016/B978-0-444-52014-2.00040-9

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

M3 - Article

C2 - 21496607

AN - SCOPUS:79954520051

SN - 0072-9752

VL - 100

SP - 559

EP - 562

JO - Handbook of Clinical Neurology

JF - Handbook of Clinical Neurology

ER -

Rapid-onset dystonia-parkinsonism

Abstract

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