Myoclonic dystonia 26

MONDO:0014620

Any myoclonus-dystonia syndrome in which the cause of the disease is a mutation in the KCTD17 gene.

Also known as: KCTD17 myoclonus-dystonia syndrome, myoclonic dystonia type 26, myoclonus-dystonia syndrome caused by mutation in KCTD17, DYT26, dystonia 26, myoclonic

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

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