Suppr超能文献

脑裂畸形:一项临床与CT研究。

Schizencephaly: a clinical and CT study.

作者信息

Miller G M, Stears J C, Guggenheim M A, Wilkening G N

出版信息

Neurology. 1984 Aug;34(8):997-1001. doi: 10.1212/wnl.34.8.997.

Abstract

Schizencephaly is a primary developmental defect of the brain, presumably caused by failure of formation of the cerebral mantle in the regions of the cerebral fissures. Identification has usually been at autopsy, in association with severe neurologic abnormalities. We identified the characteristic features of schizencephaly on CTs in 11 patients. Age at detection ranged from an infant at 8 months to a 30-year-old adult. Clinical abnormalities varied from mild to severe, including developmental delays and retardation, microcephaly, focal or generalized motor abnormalities, and seizures. CT findings included cerebral clefts, infolding of cortical gray matter along the clefts, an abnormal ventricular system, and other associated cerebral anomalies.

摘要

脑裂畸形是一种原发性脑发育缺陷,推测是由于脑沟区域的大脑皮质形成失败所致。通常在尸检时发现,伴有严重的神经功能异常。我们在11例患者的CT上识别出了脑裂畸形的特征性表现。发现时的年龄范围从8个月的婴儿到30岁的成年人。临床异常表现从轻到重各不相同,包括发育延迟和迟缓、小头畸形、局灶性或全身性运动异常以及癫痫发作。CT表现包括脑裂、沿脑裂的皮质灰质内折、异常的脑室系统以及其他相关的脑部异常。

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