Episodic kinesigenic dyskinesia 2

MONDO:0012603

A dystonia characterized by autosomal dominant inheritance of recurrent brief involuntary hyperkinesias triggered by sudden movements that has material basis in variation in the chromosome region 16q13-q22.1.

Also known as: episodic kinesigenic dyskinesia 2, episodic kinesigenic dyskinesia type 2, EKD2, dystonia 19

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

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