Suppr超能文献

胼胝体发育不全:临床描述与病因学

Agenesis of corpus callosum: clinical description and etiology.

作者信息

Marszał E, Jamroz E, Pilch J, Kluczewska E, Jabłecka-Deja H, Krawczyk R

机构信息

Pediatric Neurology Clinic, Silesian School of Medicine, Katowice, Poland.

出版信息

J Child Neurol. 2000 Jun;15(6):401-5. doi: 10.1177/088307380001500609.

Abstract

In 135 children (aged 3 months to 15 years) with structural defects of the central nervous system found on magnetic resonance imaging, agenesis of the corpus callosum was evident in 7. The etiology of agenesis of the corpus callosum has been established in four children: partial trisomy of chromosome 13, partial duplication of the long arm of chromosome 10, Aicardi's syndrome, and intracranial bleeding during the fetal period as a result of injury. Agenesis of the corpus callosum coexisted with a Dandy-Walker malformation in one other patient, which suggests a genetic etiology. In spite of these variable etiologies, dysmorphic features were identified in all seven patients, as was psychomotor retardation. Epileptic seizures had occurred in six patients, and all manifested abnormalities on neurologic examination.

摘要

在135名经磁共振成像检查发现有中枢神经系统结构缺陷的儿童(年龄在3个月至15岁之间)中,7名儿童存在胼胝体发育不全。已确定4名儿童胼胝体发育不全的病因:13号染色体部分三体、10号染色体长臂部分重复、艾卡迪综合征以及胎儿期因损伤导致的颅内出血。另有1名患者的胼胝体发育不全与丹迪-沃克畸形并存,这提示存在遗传病因。尽管病因各异,但所有7名患者均有畸形特征,且存在精神运动发育迟缓。6名患者发生过癫痫发作,且所有患者神经检查均显示异常。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验