Developmental and Epileptic Encephalopathy 32

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant form of early infantile epileptic encephalopathy, caused by mutation(s) in the KCNA2 gene, encoding potassium voltage-gated channel subfamily A member 2.

**Synonyms:** - DEE32 - EIEE32 - Early Infantile Epileptic Encephalopathy 32