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一名患有巨头畸形、神经元迁移异常和持续性嗅脑室的婴儿。

An infant with macrocephaly, abnormal neuronal migration and persistent olfactory ventricles.

作者信息

Andrews P I, Hulette C M

机构信息

Department of Pediatric Neurology, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Clin Neuropathol. 1993 Jan-Feb;12(1):13-8.

PMID:8440077
Abstract

An asphyxiated male infant was delivered by cesarean section at 38 weeks gestation. The patient was macrocephalic with clinical evidence of fetal immobility syndrome. He died aged two days. Autopsy revealed excessive brain weight, pachygyria, enlarged olfactory tracts and hypoplastic optic nerves. Microscopy revealed evidence of impaired neuronal migration throughout the cortex. The olfactory bulbs showed persistence of the primitive olfactory ventricles and absence of olfactory glomeruli. There was persistence of the fetal connection between lateral and olfactory ventricles. The lateral geniculate nuclei, inferior olivary nuclei and dentate nuclei of the cerebellum were abnormally formed. Relevant aspects of fetal brain development and clinical neuropathologic syndromes are discussed.

摘要

一名窒息男婴在妊娠38周时通过剖宫产分娩。该患者头部巨大,有胎儿运动不能综合征的临床证据。他在两天时死亡。尸检显示脑重量过重、脑回增厚、嗅束增粗和视神经发育不全。显微镜检查显示整个皮质存在神经元迁移受损的证据。嗅球显示原始嗅脑室持续存在且嗅小球缺失。外侧脑室和嗅脑室之间存在胎儿期连接持续存在。外侧膝状体核、下橄榄核和小脑齿状核形成异常。讨论了胎儿脑发育和临床神经病理综合征的相关方面。

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