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导水管闭锁作为无脑回综合征的一个特征。

Aqueductal atresia as a feature of arhinencephalic syndromes.

作者信息

Vogel H, Gessaga E C, Horoupian D S, Urich H

机构信息

Department of Pathology (Neuropathology), Stanford University Medical Center, CA 94305.

出版信息

Clin Neuropathol. 1990 Jul-Aug;9(4):191-5.

PMID:2225595
Abstract

Two cases are presented of aqueductal atresia associated with arhinencephalic syndromes. The first case was one of semilobar holoprosencephaly with occipital encephalocele, the second one of lobar holoprosencephaly (callosal agenesis with interhemispheric cyst). Only the second case was associated with obstructive hydrocephalus. The absence of hydrocephalus in the first case may be ascribed either to the greater distensibility of the encephalocele, or to the displacement of the choroid plexuses from the intracranial portion of the common ventricle into the hernial sac.

摘要

本文报告两例导水管闭锁合并无脑叶综合征的病例。第一例为半脑叶型全前脑畸形合并枕部脑膨出,第二例为脑叶型全前脑畸形(胼胝体发育不全合并半球间囊肿)。仅第二例合并梗阻性脑积水。第一例未出现脑积水可能归因于脑膨出的扩张性更强,或者脉络丛从共同脑室的颅内部分移位至疝囊内。

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