What is another word for Myoclonic Astatic Epilepsy?
Pronunciation: [mˌa͡ɪəklˈɒnɪk ɐstˈatɪk ˈɛpɪlˌɛpsi] (IPA) 
Myoclonic Astatic Epilepsy is a rare form of epilepsy that is characterized by sudden jerky movements known as myoclonic seizures and drop attacks or atonic seizures. It is also known as Doose syndrome or epilepsy with myoclonic-atonic seizures (EMAS). Other synonyms for Myoclonic Astatic Epilepsy include Grand Mal Myoclonic Epilepsy, Epileptic Encephalopathy, and Atonic-Absence Epilepsy. Although it is a rare form of epilepsy, it can be very debilitating and cause significant disruption to daily life. It often requires management with antiepileptic drugs and other supportive therapies. Awareness of this condition is important to ensure proper diagnosis and treatment.
