兰多-克莱夫纳综合症。婴儿“获得性”失语,阵发性脑电图改变和癫痫发作]。

La Nouvelle presse medicale Pub Date : 1982-12-18
M Dugas
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引用次数: 0

摘要

自从1957年Landau和Kleffner首次描述了一种仅发生在儿童身上的综合征,包括失语、脑电图的发作性改变和经常出现的癫痫发作以来,已经报道了80例。获得性语言障碍,有时与听觉失认症有关,在症状学和发展上不同于通常形式的婴儿失语症。根据失语症的消退或持续,60%的病例预后良好,40%的病例预后不良。各种抗癫痫药物中没有一种始终有效。这种综合征的病因尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The Landau-Kleffner syndrome. Infantile "acquired" aphasia, paroxysmal electroencephalographic changes and epileptic seizures].

Since the initial description by Landau and Kleffner, in 1957, of a syndrome occurring exclusively in children and consisting of aphasia, paroxysmal changes in E.E.G. and, frequently, epileptic seizures, 80 cases have been reported. The acquired speech disorder, sometimes associated with auditory agnosia, differs in symptomatology and development from the usual forms of infantile aphasia. The prognosis, based on the regression or persistence of the aphasia, is favourable in 60% of the cases and unfavourable in 40%. None of the various antiepileptic drugs is consistently effective. The cause of the syndrome remains unknown.

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