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The Landau-Kleffner Syndrome.兰道-克莱夫纳综合征
Epilepsy Curr. 2001 Nov;1(2):39-45. doi: 10.1111/j.1469-5812.2005.00134.x-i1.
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Syndrome of acquired aphasia with convulsive disorder in children.儿童获得性失语伴惊厥障碍综合征
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Landau-Kleffner syndrome: a case report.Landau-Kleffner综合征:一例报告
Neurol India. 2002 Jun;50(2):212-3.
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Successful use of intravenous immunoglobulin as initial monotherapy in Landau-Kleffner syndrome.静脉注射免疫球蛋白作为Landau-Kleffner综合征初始单一疗法的成功应用。
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Acquired aphasia in acute disseminated encephalomyelitis.急性播散性脑脊髓炎中的获得性失语
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Landau Kleffner syndrome.兰道-克莱夫纳综合征
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Language outcome following multiple subpial transection for Landau-Kleffner syndrome.兰道-克莱夫纳综合征多次软脑膜下横切术后的语言转归
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Autistic regression and disintegrative disorder: how important the role of epilepsy?自闭症退化与瓦解性障碍:癫痫的作用有多重要?
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Landau-Kleffner syndrome: consistent response to repeated intravenous gamma-globulin doses: a case report.兰道-克莱夫纳综合征:反复静脉注射丙种球蛋白剂量的一致反应:一例报告
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10
Brain single photon emission computed tomography imaging in Landau-Kleffner syndrome.大脑单光子发射计算机断层扫描成像在Landau-Kleffner综合征中的应用
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Landau-Kleffner综合征:东南亚地区一例罕见的治疗病例。

Landau-Kleffner syndrome: an uncommon dealt with case in Southeast Asia.

作者信息

Motwani Naresh, Afsar Suhaim, Dixit Nachiket S, Sharma Nitin

机构信息

Department of Paediatrics, CM Hospital and Medical College, Bhilainagar, Chhattisgarh, India.

Department of Neurology, CM Hospital, Bhilainagar, Chhattisgarh, India.

出版信息

BMJ Case Rep. 2015 Sep 29;2015:bcr2015212333. doi: 10.1136/bcr-2015-212333.

DOI:10.1136/bcr-2015-212333
PMID:26420702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4593242/
Abstract

An 11-year-old boy was admitted with fever followed by convulsions. He had developed aphasia subsequent to this illness. His birth history was unremarkable, and he had normal growth and development including of language, hearing and vision. His neurological examination was normal except for aphasia. Investigations including cerebrospinal fluid study and MRI were normal. However, EEG was abnormal and the boy was diagnosed as a case of Landau-Kleffner syndrome (LKS) and treated with sodium valproate, levetiracetam and steroids. He responded well to treatment and has been on follow-up for the last 4 months. We present this case of LKS to increase awareness about early diagnosis and to highlight the importance of appropriate management for a better outcome.

摘要

一名11岁男孩因发热后惊厥入院。患病后出现了失语症。他的出生史无异常,生长发育正常,包括语言、听力和视力方面。除失语症外,他的神经系统检查正常。包括脑脊液检查和磁共振成像在内的各项检查均正常。然而,脑电图异常,该男孩被诊断为Landau-Kleffner综合征(LKS),并接受了丙戊酸钠、左乙拉西坦和类固醇治疗。他对治疗反应良好,在过去4个月一直在接受随访。我们呈现这例LKS病例,以提高对早期诊断的认识,并强调适当管理对于获得更好预后的重要性。