Benign neonatal sleep myoclonus: case report and follow-up of four members of an affected family.

M Luigia Vaccario, Maria A Valenti, Anna Carullo, Rossella Di Bartolomeo, Salvatore Mazza
{"title":"Benign neonatal sleep myoclonus: case report and follow-up of four members of an affected family.","authors":"M Luigia Vaccario,&nbsp;Maria A Valenti,&nbsp;Anna Carullo,&nbsp;Rossella Di Bartolomeo,&nbsp;Salvatore Mazza","doi":"10.1177/155005940303400107","DOIUrl":null,"url":null,"abstract":"<p><p>Benign neonatal sleep myoclonus (BNSM), characterized by myoclonic jerks of the extremities only in non-REM sleep, occurs in the first months of life with spontaneous disappearance within 3-4 months. We examined five siblings with typical BNSM, at the 3-10 years follow-up neurological examination. Psychomotor development, cognitive functions and EEG were completely normal. These cases confirm that BNSM is a self limited and nonepileptic disorder.</p>","PeriodicalId":75713,"journal":{"name":"Clinical EEG (electroencephalography)","volume":"34 1","pages":"15-7"},"PeriodicalIF":0.0000,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/155005940303400107","citationCount":"20","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical EEG (electroencephalography)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/155005940303400107","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 20

Abstract

Benign neonatal sleep myoclonus (BNSM), characterized by myoclonic jerks of the extremities only in non-REM sleep, occurs in the first months of life with spontaneous disappearance within 3-4 months. We examined five siblings with typical BNSM, at the 3-10 years follow-up neurological examination. Psychomotor development, cognitive functions and EEG were completely normal. These cases confirm that BNSM is a self limited and nonepileptic disorder.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
良性新生儿睡眠肌阵挛:一个受影响家庭四名成员的病例报告和随访。
良性新生儿睡眠肌阵挛(BNSM),其特征是仅在非快速眼动睡眠中出现四肢肌阵挛性抽搐,发生在生命的最初几个月,在3-4个月内自然消失。我们在随访3-10年的神经学检查中检查了5例典型BNSM的兄弟姐妹。精神运动发育、认知功能及脑电图完全正常。这些病例证实BNSM是一种自限性非癫痫性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Brain Death Effects on EEG of Drugs and Toxic Substances Disorders of Consciousness Neuromonitoring and Emergency EEG EEG Signal Acquisition
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1