Myoclonic-Atonic Epilepsy

**Semantic type:** Disease or Syndrome

**Definition:** A genetically heterogenous condition characterized by early onset of absence and myoclonic seizures following developmental delay. Intellectual disability may develop following the onset of seizures.

**Synonyms:** - Doose Syndrome - MAE - Myoclonic-Astatic Epilepsy - Myoclonic-Atonic Seizure