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婴幼儿期年龄依赖性癫痫性脑病的脑电图

Electroencephalogram of age-dependent epileptic encephalopathies in infancy and early childhood.

作者信息

Wong-Kisiel Lily C, Nickels Katherine

机构信息

Division of Child and Adolescent Neurology, Department of Neurology, Mayo Clinic College of Medicine, 200 First St. SW, Rochester, MN 55905, USA.

出版信息

Epilepsy Res Treat. 2013;2013:743203. doi: 10.1155/2013/743203. Epub 2013 Aug 19.

DOI:10.1155/2013/743203
PMID:24024028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3760116/
Abstract

Epileptic encephalopathy syndromes are disorders in which the epileptiform abnormalities are thought to contribute to a progressive cerebral dysfunction. Characteristic electroencephalogram findings have an important diagnostic value in classification of epileptic encephalopathy syndromes. In this paper, we focus on electroencephalogram findings of childhood epileptic encephalopathy syndromes and provide sample illustrations.

摘要

癫痫性脑病综合征是一类疾病，其中癫痫样异常被认为会导致进行性脑功能障碍。特征性脑电图表现对癫痫性脑病综合征的分类具有重要诊断价值。在本文中，我们重点关注儿童癫痫性脑病综合征的脑电图表现并提供示例图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0759/3760116/e9845a070aa6/ERT2013-743203.019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0759/3760116/a3976e91af3c/ERT2013-743203.001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0759/3760116/e9845a070aa6/ERT2013-743203.019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0759/3760116/a3976e91af3c/ERT2013-743203.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0759/3760116/b01ca2742538/ERT2013-743203.002.jpg
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本文引用的文献

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Epileptic encephalopathies: an overview.癫痫性脑病：概述
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Epilepsy surgery for early infantile epileptic encephalopathy (ohtahara syndrome).早期婴儿癫痫性脑病（大田原综合征）的癫痫手术
J Child Neurol. 2013 Dec;28(12):1607-17. doi: 10.1177/0883073812464395. Epub 2012 Nov 8.
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De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.新生功能获得性 KCNT1 通道突变导致婴儿局灶性癫痫伴游走性阵挛。
Nat Genet. 2012 Nov;44(11):1255-9. doi: 10.1038/ng.2441. Epub 2012 Oct 21.
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Extreme delta brush: a unique EEG pattern in adults with anti-NMDA receptor encephalitis.极端德尔塔刷：抗 N- 甲基-D- 天冬氨酸受体脑炎成人患者的独特 EEG 模式。
Neurology. 2012 Sep 11;79(11):1094-100. doi: 10.1212/WNL.0b013e3182698cd8. Epub 2012 Aug 29.
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CDKL5 mutations as a cause of severe epilepsy in infancy: clinical and electroencephalographic long-term course in 4 patients.CDKL5突变作为婴儿期严重癫痫的病因：4例患者的临床及脑电图长期病程
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Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy.PLCB1 基因纯合缺失导致婴儿期恶性游走性部分性癫痫发作。
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A case of malignant migrating partial seizures in infancy as a continuum of infantile epileptic encephalopathy.一例婴儿期恶性迁移性部分性癫痫，为婴儿癫痫性脑病的一种连续表现。
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