皮质下带异位伴癫痫及言语障碍1例

Reaz Mahmud, Kazi Giasuddin Ahmed, M. Rassel
{"title":"皮质下带异位伴癫痫及言语障碍1例","authors":"Reaz Mahmud, Kazi Giasuddin Ahmed, M. Rassel","doi":"10.3329/bjn.v34i2.57555","DOIUrl":null,"url":null,"abstract":"Subcortical Heterotopia is a rare developmental disorder of human brain due to mutation in the DCX or LIS1gene.It is predominantly a disease of female. It usually present with refractory seizure and varying degree of mental retardation. Here a case of 22 years lady who presented with refractory seizure is reported. Her MRI revealed Double cortex and her EEG revealed Frontal intermittent rhythmic delta activity (FIRDA).\nBangladesh Journal of Neuroscience 2018; Vol. 34 (2): 106-109","PeriodicalId":8727,"journal":{"name":"Bangladesh Journal of Neuroscience","volume":"58 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Case of Subcortical Band Heterotopia Presented with Epilepsy and Speech Regression\",\"authors\":\"Reaz Mahmud, Kazi Giasuddin Ahmed, M. Rassel\",\"doi\":\"10.3329/bjn.v34i2.57555\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Subcortical Heterotopia is a rare developmental disorder of human brain due to mutation in the DCX or LIS1gene.It is predominantly a disease of female. It usually present with refractory seizure and varying degree of mental retardation. Here a case of 22 years lady who presented with refractory seizure is reported. Her MRI revealed Double cortex and her EEG revealed Frontal intermittent rhythmic delta activity (FIRDA).\\nBangladesh Journal of Neuroscience 2018; Vol. 34 (2): 106-109\",\"PeriodicalId\":8727,\"journal\":{\"name\":\"Bangladesh Journal of Neuroscience\",\"volume\":\"58 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-07-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bangladesh Journal of Neuroscience\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3329/bjn.v34i2.57555\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bangladesh Journal of Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/bjn.v34i2.57555","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

皮层下异位症是由DCX或lis1基因突变引起的一种罕见的人类大脑发育障碍。它主要是女性的疾病。它通常表现为难治性癫痫发作和不同程度的智力迟钝。本文报告一位22岁的女性,以难治性癫痫发作为表现。MRI显示双皮质,脑电图显示额叶间歇节律性三角洲活动(FIRDA)。孟加拉国神经科学杂志2018;Vol. 34 (2): 106-109
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Subcortical Band Heterotopia Presented with Epilepsy and Speech Regression
Subcortical Heterotopia is a rare developmental disorder of human brain due to mutation in the DCX or LIS1gene.It is predominantly a disease of female. It usually present with refractory seizure and varying degree of mental retardation. Here a case of 22 years lady who presented with refractory seizure is reported. Her MRI revealed Double cortex and her EEG revealed Frontal intermittent rhythmic delta activity (FIRDA). Bangladesh Journal of Neuroscience 2018; Vol. 34 (2): 106-109
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信