MeSH Browser

MeSH Supplementary: Dystonia, Dopa-responsive
Unique ID: C538007
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538007
Entry Term(s): Dopa-Responsive Dystonia; Dopa-responsive dystonia, autosomal dominant; Dystonia 5; Dystonia, Dopa-responsive, autosomal dominant; Dystonia, progressive, with diurnal variation; Dystonia-Parkinsonism with diurnal fluctuation; Hereditary Progressive Dystonia with Marked Diurnal Fluctuation; Segawa syndrome, autosomal dominant
Registry Numbers: 0
Heading Mapped to: *Dystonic Disorders
Frequency: 118
Note: A hereditary DYSTONIA where symptoms similar to those of PARKINSON DISEASE arise in early childhood; it responds favorably to treatment with LEVODOPA. Germline mutations in the GCH1 gene have been identified. OMIM: 128230
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Dystonia, Dopa-responsive MeSH Supplementary Concept Data 2025