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青少年胱氨酸病:对一个特殊家系的临床及镜检研究

Adolescent cystinosis: a clinical and specular microscopic study of an unusual sibship.

作者信息

Dale R T, Rao G N, Aquavella J V, Metz H S

出版信息

Br J Ophthalmol. 1981 Dec;65(12):828-32. doi: 10.1136/bjo.65.12.828.

Abstract

Six members of a sibship originally consisting of 8 offspring lived to teenage. Five of these developed the adolescent form of cystinosis. Since adolescent cystinosis is autosomal recessive, such a high incidence of affected members is of uncommon occurrence. Depending on whether the sibship size (n) is known as 6 to 8, it should occur only in approximately 1.5% or 5.8% of sibships of corresponding size. Specular microscopy was used to study the corneal stroma of all 3 of the living, affected members of this sibship and the conjunctiva of one of the siblings. Vivid, needle-shaped crystals were observed in the corneal stroma. Smaller, variably shaped crystals were observed in the conjunctiva. The crystals seen with specular microscopy fit the description of those studied with light and electron microscopy.

摘要

一个最初由8个后代组成的同胞家族中有6人活到了青少年期。其中5人患上了青少年型胱氨酸病。由于青少年型胱氨酸病是常染色体隐性遗传,受影响成员如此高的发病率并不常见。根据同胞家族大小(n)已知为6至8,这种情况应该只在相应大小的同胞家族中约1.5%或5.8%的家族中出现。使用镜面显微镜研究了这个同胞家族中所有3名在世的受影响成员的角膜基质以及其中一名同胞的结膜。在角膜基质中观察到了生动的针状晶体。在结膜中观察到了较小的、形状各异的晶体。镜面显微镜下看到的晶体与用光镜和电镜研究的晶体描述相符。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f48/1039689/2f05459ed51e/brjopthal00192-0038-a.jpg

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