Dystonia 28, childhood-onset

MONDO:0015004

Any dystonic disorder in which the cause of the disease is a mutation in the KMT2B gene.

Also known as: DYT28, KMT2B dystonic disorder, dystonia 28, childhood-onset, dystonia 28, childhood-onset; DYT28, dystonic disorder caused by mutation in KMT2B

14 clinical trials for this condition and its sub-types.

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