Suppr超能文献

[A special case of 'deafness'; Landau-Kleffner syndrome].

作者信息

Stroink H, Van Dongen H R, Meulstee J, Scheltens-de Boer M, Geesink H H

机构信息

Afd. Kinderneurologie, Academisch Ziekenhuis Rotterdam-Sophia Kinderziekenhuis.

出版信息

Ned Tijdschr Geneeskd. 1997 Aug 16;141(33):1623-5.

PMID:9543768
Abstract

A boy aged 5 had displayed from the age of 3 a fluctuating deficit in understanding spoken language. Audiometric testing proved his hearing to be normal. After 18 months, the parents noticed minor attacks of 'absence'. An EEG showed a normal background pattern and frequent spikes and spike waves complexes; CT-scanning of the brain revealed no abnormalities. On the basis of the acquired language disorder, the seizures and the features of the nocturnal EEG, the diagnosis the syndrome of Landau-Kleffner was made. After treatment with ethosuximide a temporary improvement of the aphasia occurred. A permanent improvement however was realized by treatment with prednisone. The boy could attend a primary school. The syndrome runs a fluctuating course; the patient may recover, but he may also undergo general mental deterioration. Antiepileptic agents only may have a brief favorable effect on the aphasia. In case of failure corticosteroids or even subpial cortical transsection are indicated.

摘要

相似文献

1
[A special case of 'deafness'; Landau-Kleffner syndrome].
Ned Tijdschr Geneeskd. 1997 Aug 16;141(33):1623-5.
8
Specific language impairment versus Landau-Kleffner syndrome.特定语言障碍与兰道-克莱夫纳综合征
Epilepsia. 2009 Aug;50 Suppl 7:21-4. doi: 10.1111/j.1528-1167.2009.02213.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验