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圆锥角膜和蓝色巩膜。

Keratoglobus and blue sclera.

作者信息

Biglan A W, Brown S I, Johnson B L

出版信息

Am J Ophthalmol. 1977 Feb;83(2):225-33. doi: 10.1016/0002-9394(77)90621-3.

Abstract

Five patients from two families had similar features including keratoglobus, blue scleras, hyperextensibility of the hand, wrist, and ankle joints, sensorineural conduction hearing alterations, and mottling of the teeth. Keratoglobus had been observed in all patients at, or shortly after, birth. Corneal perforations developed in seven of the ten eyes after minimal trauma. Repair of these perforations was complicated by the extremely thin corneas and six eyes had to be either enucleated or eviscerated. Histopathological examination of two of the enucleated eyes showed the corneal stromas of both eyes to be estremely thin, Bowman's membrane was absent, and Descemet's membrane was unusually thick. This condition has an autosomal-recessive inheritance pattern.

摘要

来自两个家族的五名患者具有相似的特征,包括球形角膜、蓝色巩膜、手部、腕部和踝关节的过度伸展性、感觉神经性传导听力改变以及牙齿斑纹。所有患者在出生时或出生后不久就出现了球形角膜。十只眼中有七只在受到轻微创伤后发生了角膜穿孔。由于角膜极薄,这些穿孔的修复很复杂,六只眼睛不得不被摘除或眼内容剜出。对两只摘除眼球的组织病理学检查显示,两只眼睛的角膜基质都极薄,Bowman膜缺失,Descemet膜异常增厚。这种疾病具有常染色体隐性遗传模式。

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