Literature DB >> 6851297

Iniencephaly: a neuropathologic study.

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

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.

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Mesh:

Year:  1983        PMID: 6851297

Source DB:  PubMed          Journal:  Clin Neuropathol        ISSN: 0722-5091            Impact factor:   1.368


  3 in total

1.  Iniencephaly with mediastinal bronchogenic cyst: A case report.

Authors:  Yeşim Akdemir; Habibe Ayvacı; Oya Demirci; Davut Sahin; Ersan Demirağ; Hamdullah Sözen; Mehmet Uludoğan
Journal:  J Prenat Med       Date:  2010-10

2.  Iniencephaly and long-term survival: a rare case report.

Authors:  Murat Hamit Aytar; Fikret Doğulu; Berker Cemil; Ertan Ergün; Gökhan Kurt; Kemali Baykaner
Journal:  Childs Nerv Syst       Date:  2007-03-16       Impact factor: 1.475

3.  Exencephaly in Cantrell-Haller-Ravitsch Syndrome.

Authors:  A Hori; U Roessmann; R Eubel; R Ulbrich; B Dietrich-Schott
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

  3 in total

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