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伴有基底脑膨出的隐眼综合征

Cryptophthalmos syndrome with basal encephaloceles.

作者信息

Goldhammer Y, Smith J L

出版信息

Am J Ophthalmol. 1975 Jul;80(1):146-9. doi: 10.1016/0002-9394(75)90885-5.

Abstract

A 2,144-g white girl was born with absence of the right ear and eye, cleft lip and palate, two basal encephaloceles, tricuspid atresia, ventricualr and atrial septal defects, detransposition of the great vessels, right aortic arch, and aberrant right subclavian artery. Through an oval defect in the center of the sphenoid bone, soft tissue protruded into the right nasopharynx. The medial portions of the roof of both orbits and the cribriform plate were absent and soft tissue protruded through this bony defect. Basal tomography was required to demonstrate the encephaloceles, which should be suspected in any child with a median cleft syndrome, a flat broad nasal root, and hypertelorism.

摘要

一名体重2144克的白人女婴出生时即存在右耳和右眼缺失、唇腭裂、两个基底脑膨出、三尖瓣闭锁、心室和房间隔缺损、大血管转位、右位主动脉弓以及迷走右锁骨下动脉。通过蝶骨中心的椭圆形缺损,软组织突入右侧鼻咽部。双侧眶顶和筛板的内侧部分缺失,软组织通过该骨缺损突出。需要进行基底层面体层摄影来显示脑膨出,对于任何患有正中裂综合征、扁平宽阔鼻根和眼距过宽的儿童都应怀疑有脑膨出。

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