Sturge-Weber/Klippel-Trenaunay综合征患儿的短暂性偏瘫

J. Godoy, A. Godoy
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引用次数: 0

摘要

本研究旨在描述一名患者的神经系统进化与斯特奇-韦伯综合征和克里佩尔-特伦纳韦综合征的关联。我们报告了一个女孩出生时,整个身体都有葡萄酒色的病变。这名儿童后来出现了两次神经性发作;第二种疗法使病人半身瘫痪,失去意识,不能说话。患者在第7天开始恢复,但完全恢复需要一个多月的时间,在此期间可以观察到脑灌注的改善和恶化。目前患者23岁,上大学,身体健康,无明显神经症状。关键词:Sturge-Weber综合征- klippel - trenaunay综合征-偏瘫
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transient hemiplegia in a child with Sturge-Weber/Klippel-Trenaunay syndrome
This study was to describe the neurological evolution of a patient an association ofSturge-Weber and Klippel-Trenaunay syndromes. We report on a girl who was bornwith port wine-colored lesions over the entire body. The child later suffered two neurologicalepisodes; the second left the patient hemiplegic, without consciousness andunable to speak. She started to recover after the seventh day, however full recoverytook more than one month during which time periods of improvement and deteriorationof cerebral perfusion were detected. Currently the patient is 23 years old, attendeda college and is well without obvious neurological signs.Key words: Sturge-Weber syndrome–Klippel-Trenaunay syndrome–hemiplegia
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