Suppr超能文献

一例罕见的婴儿良性反射性肌阵挛癫痫病例。

An unusual case of benign reflex myoclonic epilepsy of infancy.

作者信息

Kurian M A, King M D

机构信息

Department of Paediatric Neurology, The Children's Hospital, Dublin, Eire.

出版信息

Neuropediatrics. 2003 Jun;34(3):152-5. doi: 10.1055/s-2003-41275.

Abstract

A previously healthy one-year-old boy, the youngest child of unrelated parents, presented with a four-week history of episodes of myoclonus triggered only by tactile stimulation to his head. There had been no loss of developmental skills. The electroencephalogram (EEG) revealed generalised polyspike wave activity both with and without clinical correlate. The infant was started on sodium valproate, which resulted in cessation of the myoclonic episodes one week after starting therapy. At subsequent follow-up (at 18 months) the infant was seizure free and a repeat EEG was normal. This case of non-progressive reflex myoclonic epilepsy of infancy triggered only by head tapping (and not by acoustic stimuli) is an extremely rare phenomenon. Reflex myoclonic epilepsy of infancy represents a distinct subtype of myoclonic epilepsy in infancy. It should be considered as an age-dependent idiopathic generalised epileptic syndrome with an apparently good prognosis.

摘要

一名此前健康的一岁男童,是父母非近亲的最小孩子,出现了仅由头部触觉刺激引发的为期四周的肌阵挛发作史。其发育技能未丧失。脑电图(EEG)显示,无论有无临床相关性,均存在全身性多棘波活动。该婴儿开始服用丙戊酸钠,治疗一周后肌阵挛发作停止。在随后的随访(18个月时)中,婴儿无癫痫发作,复查脑电图正常。这种仅由轻拍头部(而非听觉刺激)引发的非进行性婴儿反射性肌阵挛癫痫病例极为罕见。婴儿反射性肌阵挛癫痫是婴儿肌阵挛癫痫的一种独特亚型。它应被视为一种年龄依赖性特发性全身性癫痫综合征,预后明显良好。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验