期刊
NEUROLOGY
卷 82, 期 24, 页码 2250-2251出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000000521
关键词
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Dravet syndrome (DS) is a severe genetic epileptic encephalopathy mainly caused by SCN1A mutations.(1) Children usually develop frequent and pharmacoresistant seizures of several types. Besides cognitive delay, some patients later develop gait ataxia. Crouch gait has also been described in older patients.(2,3
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