Epilepsy, progressive myoclonic, 1B

MONDO:0012904

Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the PRICKLE1 gene.

Also known as: PRICKLE1 progressive myoclonic epilepsy, epilepsy, progressive myoclonic 1B, epilepsy, progressive myoclonic, 1B, epilepsy, progressive myoclonic, type 1B, progressive myoclonic epilepsy caused by mutation in PRICKLE1, EPM1B

7 clinical trials for this condition and its sub-types, 0 tagged with Epilepsy, progressive myoclonic, 1B itself.

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↑ Progressive myoclonus epilepsy (12)

Including sub-types (7) Tagged with Epilepsy, progressive myoclonic, 1B (0)

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