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[一种不明眼脑异常综合征的临床及组织病理学发现]

[Clinical and histopathological findings in an unknown oculocerebral abnormality syndrome].

作者信息

Strempel I

出版信息

Ophthalmologica. 1984;188(4):197-207. doi: 10.1159/000309363.

Abstract

2 brothers of a genetically healthy family were born with multiple identical malformations and died at the age of 11 and 15 years. Clinically they presented hydrocephalus with convulsions, spastic dysplegia and blindness. Ophthalmologic investigations revealed one macrophthalmic eye with retinal malformations and deeply pigmented, partly occluded choroid, abnormal scleral pigmentation and optic atrophy. The other small eye showed meso- and ectodermal dysgenesis of the anterior segment and total retinal detachment as well as optic dysplasia. The brain was remarkably abnormal as well.

摘要

一个基因健康的家庭中有两兄弟,出生时患有多种相同的畸形,并分别在11岁和15岁时死亡。临床上,他们表现为脑积水伴惊厥、痉挛性双下肢瘫和失明。眼科检查发现,一只眼睛眼球增大,伴有视网膜畸形,脉络膜色素沉着深且部分闭塞,巩膜色素沉着异常以及视神经萎缩。另一只小眼睛表现为眼前节中胚层和外胚层发育异常、视网膜完全脱离以及视神经发育不良。大脑也明显异常。

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