肌阵挛-失张力癫癎(Doose综合征)1例报告
摘要
肌阵挛-失张力癫癎(epilepsy with myoclonic-atonic seizures,EMAs),又称Doose综合征。Doose等1970年首次描述了EMAS的临床特征,1989年国际抗癫癎联盟(ILAE)将其归类为“隐源性和(或)症状性全面性癫癎”,2010年ILAE在关于癫癎发作、综合征分类及术语报告中将EMAS列为按年龄分类的电临床综合征中儿童期的一种。
出处
《癫痫与神经电生理学杂志》
2014年第3期187-189,共3页
Journal of Epileptology and Electroneurophysiology(China)
参考文献14
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共引文献9
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1张丹,吴立文.肌阵挛-失张力癫痫研究进展[J].中华神经科杂志,2011,44(10):711-712. 被引量:3
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2邓劼,张月华,杨志仙,刘晓燕,熊晖,王爽,姜玉武,秦炯,吴希如.肌阵挛失张力癫痫48例治疗及预后随访[J].中国实用儿科杂志,2012,27(1):57-61. 被引量:7
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3王丽君,陈银波,林卫红,梁东.肌阵挛-失张力癫痫1例追踪随访及文献复习[J].中风与神经疾病杂志,2012,29(1):82-83. 被引量:1
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4秦炯.儿童神经系统疾病研究进展[J].中国实用儿科杂志,2012,27(5):360-363. 被引量:6
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