Developmental and Epileptic Encephalopathy 28

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal recessive subtype of developmental and epileptic encephalopathy caused by mutation(s) in the WWOX gene, encoding WW domain-containing oxidoreductase.

**Synonyms:** - DEE28 - EIEE28 - Early Infantile Epileptic Encephalopathy 28