Seizures, benign familial infantile, 3

Any benign familial infantile epilepsy in which the cause of the disease is a mutation in the SCN2A gene.

Also known as: BFNIS, SCN2A benign familial infantile epilepsy, benign familial infantile epilepsy caused by mutation in SCN2A, benign familial neonatal-infantile seizures, benign neonatal-infantile epilepsy, seizures, benign familial infantile, 3, seizures, benign familial infantile, type 3, BFIS3

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