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进行性施奈德角膜营养不良。

Progressive Schnyder's corneal dystrophy.

作者信息

Ingraham H J, Perry H D, Donnenfeld E D, Donaldson D D

机构信息

Department of Ophthalmology, Geisinger Medical Center, Danville, Pennsylvania 17822-2120.

出版信息

Ophthalmology. 1993 Dec;100(12):1824-7. doi: 10.1016/s0161-6420(93)31391-6.

Abstract

BACKGROUND

Schnyder's crystalline dystrophy is a central anterior bilateral corneal dystrophy characterized by the deposition of crystals composed of cholesterol and other lipids. This condition classically is described as nonprogressive after childhood, but a series of recent studies following patients over time has challenged this teaching.

PATIENTS

The authors present a family pedigree including a patient first reported in 1954 and followed for 25 years with dramatic progression of the corneal condition in a dense, discoid pattern of crystals. Best-corrected visual acuity decreased from 20/30 to 20/80 in both eyes. This patient now has three children, all with typical corneal involvement.

RESULTS

Ocular pathologic examination performed on corneal biopsies submitted for light and electron microscopy demonstrated cholesterol deposition consistent with a diagnosis of Schnyder's.

CONCLUSION

Schnyder's corneal dystrophy may progress significantly over time. The characterization of this condition as stationary may need to be reconsidered.

摘要

背景

施奈德结晶性角膜营养不良是一种中央前部双侧角膜营养不良,其特征是由胆固醇和其他脂质组成的晶体沉积。这种病症传统上被描述为儿童期后无进展,但最近一系列对患者进行长期随访的研究对这一观点提出了挑战。

患者

作者展示了一个家族谱系,其中包括一名于1954年首次报告的患者,并对其进行了25年的随访,其角膜病情呈密集盘状晶体模式急剧进展。双眼最佳矫正视力从20/30降至20/80。该患者现有三个孩子,均有典型的角膜受累。

结果

对提交用于光镜和电镜检查的角膜活检组织进行的眼部病理检查显示胆固醇沉积,符合施奈德病的诊断。

结论

施奈德角膜营养不良可能随时间显著进展。可能需要重新考虑将这种病症描述为静止性的观点。

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