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首页> 外文期刊>Brain & Development >Occurrence of bilaterally independent epileptic spasms after a corpus callosotomy in West syndrome
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Occurrence of bilaterally independent epileptic spasms after a corpus callosotomy in West syndrome

机译:西部综合征call体切开术后双侧独立性癫痫痉挛的发生

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摘要

We report a patient with intractable West syndrome whose epileptic spasms (ESs) were initially bilaterally synchronous, as is typical; after a complete corpus callosotomy, however, bilaterally independent ESs originated in either hemisphere. Activity of probable cortical origin associated with ESs was detected by observing ictal gamma oscillations. Brain MRI revealed no structural abnormality before surgery. This case suggests that ESs with a hemispheric origin may appear generalized because of synchronizing effects in the corpus callosum in some patients. (c) 2015 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.
机译:我们报告一位患有顽固性West综合征的患者,其癫痫痉挛(ESs)最初是典型的双边同步性;但是,在完全体切开术之后,双边独立的ES起源于任一半球。通过观察太阳伽马振荡来检测可能与ES相关的皮质起源活动。脑部MRI显示术前无结构异常。这种情况表明,由于某些患者call体中的同步效应,具有半球起源的ES可能显得泛化。 (c)2015年日本儿童神经病学会。由Elsevier B.V.发布。保留所有权利。

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