Developmental and epileptic encephalopathy, 49

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the DENND5A gene.

Also known as: DEE49, DENND5A early infantile epileptic encephalopathy, EIEE49, developmental and epileptic encephalopathy 49, early infantile epileptic encephalopathy caused by mutation in DENND5A, epileptic encephalopathy, early infantile, 49, epileptic encephalopathy, early infantile, 49; EIEE49, epileptic encephalopathy, early infantile, type 49

17 clinical trials for this condition and its sub-types, 0 tagged with Developmental and epileptic encephalopathy, 49 itself.