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 | |
State | Published - 2011 |
ASJC Scopus subject areas
- Neurology
- Clinical Neurology