Epilepsy, early-onset, vitamin B6-dependent

MONDO:0015005

A pyridoxine-dependent epilepsy that has material basis in homozygous or compound heterozygous mutation in the PLPBP gene on chromosome 8p11.23.

Also known as: EPVB6D, epilepsy, early-onset, vitamin B6-dependent, epilepsy, early-onset, vitamin B6-dependent; EPVB6D

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

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