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马梅内先天性遗传性角膜水肿:其临床特征、治疗及病理学

Congenital hereditary corneal oedema of Maumenee: its clinical features, management, and pathology.

作者信息

Kirkness C M, McCartney A, Rice N S, Garner A, Steele A D

出版信息

Br J Ophthalmol. 1987 Feb;71(2):130-44. doi: 10.1136/bjo.71.2.130.

Abstract

The clinical and histological features of congenital hereditary corneal oedema in 23 patients are presented. The series includes cases of both recessive and dominant inheritance. Although the condition is present at birth or in early childhood, visual development appears to be little impaired, if at all. Penetrating keratoplasty carries a relatively good surgical prognosis and can produce a substantial visual gain even when carried out late in life.

摘要

本文介绍了23例先天性遗传性角膜水肿的临床和组织学特征。该系列包括隐性和显性遗传病例。虽然该病在出生时或儿童早期就已存在,但视觉发育似乎很少受到损害,即便有损害也很轻微。穿透性角膜移植术具有相对良好的手术预后,即使在晚年进行,也能显著提高视力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/416e/1041104/d0621bfcc658/brjopthal00612-0057-a.jpg

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