Progressive myoclonic epilepsy type 7

MONDO:0014521

Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the KCNC1 gene.

Also known as: EPM7, KCNC1 progressive myoclonic epilepsy, MEAK, PME type 7, epilepsy, progressive myoclonic type 7, meak, myoclonus epilepsy and ataxia due to potassium channel mutation, progressive myoclonic epilepsy caused by mutation in KCNC1

19 clinical trials for this condition and its sub-types, 0 tagged with Progressive myoclonic epilepsy type 7 itself.

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Part of

↑ Movement disorder (805) ↑ Progressive myoclonus epilepsy (12)

Including sub-types (19) Tagged with Progressive myoclonic epilepsy type 7 (0)

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