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原发性家族性角膜淀粉样变性

Primary familial amyloidosis of the cornea.

作者信息

Stock E L, Kielar R A

出版信息

Am J Ophthalmol. 1976 Aug;82(2):266-71. doi: 10.1016/0002-9394(76)90432-3.

Abstract

A case of primary familial amyloidosis of the cornea in a 13-year-old boy was confirmed by histopathologic examination of material obtained by penetrating keratoplasty. Elevated subepithelial nodules of amyloid were present centrally. Extensive nonelevated subepithelial amyloid deposition was present in areas where either clinically gray, nonelevated subepithelial opacities or apparently normal cornea was present. Nonelevated subepithelial corneal deposits clinically similar to amyloid deposits in the proband were present in two siblings. The genetic pattern of the corneal amyloid deposits in this family appears to be autosomal recessive. Cataracts were present in two of the three affected members. Aspirated lens material from two of the affected members did not contain amyloid.

摘要

一名13岁男孩原发性家族性角膜淀粉样变性病例经穿透性角膜移植获取材料的组织病理学检查得以确诊。中央可见上皮下淀粉样蛋白结节隆起。在临床呈现灰色、上皮下无隆起混浊或看似正常角膜的区域,存在广泛的上皮下非隆起性淀粉样蛋白沉积。该先证者的两名同胞出现临床上与角膜淀粉样蛋白沉积相似的上皮下非隆起性角膜沉积物。这个家族中角膜淀粉样蛋白沉积的遗传模式似乎是常染色体隐性遗传。三名受影响成员中有两名患有白内障。两名受影响成员吸出的晶状体材料中未发现淀粉样蛋白。

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