MeSH Browser

MeSH Supplementary: Paroxysmal nonkinesigenic dyskinesia
Unique ID: C537181
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537181
Entry Term(s): Choreoathetosis familial paroxysmal; Choreoathetosis, Familial Paroxysmal; Choreoathetosis, Nonkinesigenic; Dystonia 8; Familial Paroxysmal Nonkinesigenic Dyskinesia; Familial paroxysmal choreoathetosis; Mount-Reback syndrome; Nonkinesigenic choreoathetosis; Paroxysmal Nonkinesigenic Dyskinesia 1; Paroxysmal dystonic choreoathetosis
Heading Mapped to: *Chorea
Frequency: 32
Note: A hereditary autosomal dominant disorder characterized by episodes of involuntary movements involving the extremities, neck, trunk, or face. Onset is usually in infancy or childhood and episodes may be precipitated by alcohol, caffeine, fatigue, or stress. Mutations in the PNKD gene have been identified. OMIM: 118800
Date of Entry: 2010/11/13
Revision Date: 2015/08/18

Paroxysmal nonkinesigenic dyskinesia MeSH Supplementary Concept Data 2024