Developmental and epileptic encephalopathy, 37

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the FRRS1L gene.

Also known as: DEE37, EIEE37, FRRS1L early infantile epileptic encephalopathy, developmental and epileptic encephalopathy 37, early infantile epileptic encephalopathy caused by mutation in FRRS1L, epileptic encephalopathy, early infantile, 37, epileptic encephalopathy, early infantile, 37; EIEE37, epileptic encephalopathy, early infantile, type 37

17 clinical trials for this condition and its sub-types, 0 tagged with Developmental and epileptic encephalopathy, 37 itself.