Epilepsy, progressive myoclonic, 1B

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.