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Iniencephaly: a neuropathologic study.

作者信息

Aleksic S, Budzilovich G, Greco M A, Feigin I, Epstein F, Pearson J

出版信息

Clin Neuropathol. 1983;2(2):55-61.

PMID:6851297
Abstract

Five cases of iniencephaly are reviewed. Numerous central nervous system malformations were found at all levels, including microencephaly, polymicrogyria, heterotopic glial tissue in the leptomeninges, atresia of the ventricular system, marked disorganization of the brain stem, vermian agenesis, large cerebellar cyst, and disorganization of the spinal cord tissue. The cerebellum was normal in one case. Numerous skeletal anomalies were found as well as marked retroflexion of the craniocervical junction. We concluded that cerebral anomalies, although severe, are not specific for iniencephaly. Cerebellar anomalies, on the other hand, were considered to share some morphologic features between Dandy-Walker and Arnold-Chiari, i.e., Chiari type II and Chiari type III, malformations.

摘要

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引用本文的文献

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A Rare Case of Fetal Neural Tube Defect; Iniencephaly Clausus.一例罕见的胎儿神经管缺陷;隐性脊柱裂头畸形。
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Iniencephaly with mediastinal bronchogenic cyst: A case report.无脑儿合并纵隔支气管源性囊肿:一例报告。
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Iniencephaly and long-term survival: a rare case report.无脑儿与长期生存:一例罕见病例报告
Childs Nerv Syst. 2007 Jun;23(6):719-21. doi: 10.1007/s00381-007-0309-6. Epub 2007 Mar 16.
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Exencephaly in Cantrell-Haller-Ravitsch Syndrome.
Acta Neuropathol. 1984;65(2):158-62. doi: 10.1007/BF00690470.