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Early myoclonic encephalopathy : ウィキペディア英語版
Early myoclonic encephalopathy

Early myoclonic encephalopathy (EME) is an epilepsy syndrome where myoclonic seizures develop in the neonatal period. After several months, the seizure pattern may develop to infantile spasms (West syndrome). Various genetic and metabolic disorders are responsible. The seizures are resistant to treatment. The neurology is very abnormal and patients often do not live beyond one year.〔〔
==References==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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