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Myoclonic astatic epilepsy, also known as Doose syndrome, is a generalized idiopathic epilepsy. It is characterized by the development of myoclonic seizures and/or myoclonic astatic seizures. ==Signs and symptoms== Tonic–clonic Seizures with repetitive sequences of stiffening and jerking of the extremities. Myoclonic Seizures with rapid, brief contractions of muscles. Atonic Seizures with a sudden loss of muscle tone, often resulting in sudden collapse. These are also called drop seizures. Absence A generalized seizure characterized by staring off and occasionally some orofacial automatisms. 〔https://www.seizuretracker.com/〕 Myoclonic astatic Seizures that involve a myoclonic seizure followed immediately by an atonic seizure. This type of seizure is exclusive to MAE and is one of the defining characteristics of this syndrome. Tonic Muscle stiffening or rigidity. This seizure is rare in this syndrome. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Myoclonic astatic epilepsy」の詳細全文を読む スポンサード リンク
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