Autosomal dominant dopa-responsive dystonia

MONDO:0971063

A rare neurometabolic disorder characterized by childhood-onset dystonia that shows a dramatic and sustained response to low doses of levodopa (L-dopa) and that may be associated with parkinsonism at an older age.

14 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant dopa-responsive dystonia itself.

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Where it sits in the disease tree

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Part of

↑ Inborn errors of metabolism (2231) ↑ Inherited dystonia (36) ↑ Dopa-responsive dystonia (2)

Sub-types of Autosomal dominant dopa-responsive dystonia

Dystonia 5 0 trials
Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism 0 trials
1 sub-type
- Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to a NR4A2 point mutation 0 trials

Including sub-types (14) Tagged with Autosomal dominant dopa-responsive dystonia (0)

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