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胼胝体发育不全的谱系

Spectrum of corpus callosum agenesis.

作者信息

Sztriha László

机构信息

Department of Paediatrics, Faculty of Medicine and Health Sciences, UAE University, Al Ain, United Arab Emirates.

出版信息

Pediatr Neurol. 2005 Feb;32(2):94-101. doi: 10.1016/j.pediatrneurol.2004.09.007.

Abstract

Magnetic resonance imaging and clinical features of 16 children with agenesis of the corpus callosum are reviewed. The patients were classified in three groups. Eight children had agenesis of the corpus callosum without substantial involvement of other brain areas. This group included patients with interhemispheric cyst, lipoma, or partial agenesis (hypogenesis) of the corpus callosum. Four patients in the second group manifested severe telencephalic dysgenesis in addition to agenesis of the corpus callosum. In the third group, agenesis of the corpus callosum was a component of a syndrome in four children. The outcome was not favorable for the majority of patients, even in the first group without significant involvement of other systems. Severe handicaps with developmental delay, intellectual disability, and neurologic deficit were observed in patients with additional telencephalic dysgenesis or syndromic form of corpus callosum agenesis.

摘要

回顾了16例胼胝体发育不全儿童的磁共振成像和临床特征。患者被分为三组。8名儿童患有胼胝体发育不全,未累及其他脑区。该组包括患有半球间囊肿、脂肪瘤或胼胝体部分发育不全(发育不良)的患者。第二组中有4名患者除胼胝体发育不全外,还表现出严重的端脑发育不全。在第三组中,4名儿童的胼胝体发育不全是综合征的一部分。即使在第一组未累及其他系统的患者中,大多数患者的预后也不理想。在伴有额外端脑发育不全或综合征形式的胼胝体发育不全的患者中,观察到严重的发育迟缓、智力残疾和神经功能缺损等障碍。

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