Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to a NR4A2 point mutation

MONDO:0971062

An intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism in which the cause of the disease is a point mutation in the gene NR4A2.

14 clinical trials for this condition and its sub-types, 0 tagged with Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to a NR4A2 point mutation itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism (0)

Including sub-types (14) Tagged with Developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to a NR4A2 point mutation (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.