Episodic kinesigenic dyskinesia 2
MONDO:0012603A 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
14 clinical trials for this condition and its sub-types, 0 tagged with Episodic kinesigenic dyskinesia 2 itself.
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