HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

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.
AuthorsHoward L Geyer, Susan B Bressman
JournalHandbook of clinical neurology (Handb Clin Neurol) Vol. 100 Pg. 559-62 ( 2011) ISSN: 0072-9752 [Print] Netherlands
PMID21496607 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2011 Elsevier B.V. All rights reserved.
Topics
  • Diagnosis, Differential
  • Dystonic Disorders (diagnosis, genetics, therapy)
  • Humans

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: