澳大利亚大都市社区双目法定失明的原因。

Australian journal of ophthalmology Pub Date : 1983-11-01
F M Yeates
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引用次数: 0

摘要

澳大利亚法定失明定义为双眼矫正视力低于6/60;如果视敏度高于此,则可能包括附带视力损害。因此受影响的人有资格领取无效养恤金(失明)。从1975年10月到1982年6月,我研究了311例法定失明患者的临床资料,并记录了诊断结果。我亲自检查了其中259人,一名医学同事检查了52人。考生居住在澳大利亚布里斯班(或周边地区)。11人有不对称条件(单独分析),300人有对称条件。后者的病因包括遗传(20.3%)、成人黄斑病变(18%)、先天性(12.7%)、血管性(非糖尿病)(8.7%)、成人青光眼(8.3%)、糖尿病(7.3%)、外伤(6%)和其他(18.7%)。61例对称遗传病因为视网膜色素变性(34.4%)、先天性白内障(16.4%)、视网膜营养不良及黄斑病变(13.1%)、Leber’s视神经萎缩(9.8%)及其他(26.3%)。这些结果表明,应该更多地关注遗传咨询。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Causes of binocular legal blindness in an australian metropolitan community.

Australian legal blindness is defined as bilateral corrected visual acuity less than 6/60; if visual acuity is better than this, collateral visual impairments may be included. Persons thus affected qualify for the Invalid Pension (Blindness). From October 1975 to June 1982, I studied clinical data of 311 persons assessed as legally blind, and recorded diagnoses. I personally examined 259 of these persons and a medical colleague examined 52. Examinees were resident in Brisbane (or environs), Australia. Eleven persons had asymmetrical conditions (analysed separately), and 300 had symmetrical conditions. Causes of the latter were genetically transmissible (20.3%), adult maculopathy (18%), congenital (12.7%), vascular (non-diabetic) (8.7%), adult glaucoma (8.3%), diabetes (7.3%), trauma (6%), and others (18.7%). Of 61 symmetrical genetic cases causes were retinitis pigmentosa (34.4%), congenital cataracts (16.4%), retinal dystrophy and maculopathy (13.1%), Leber's optic atrophy (9.8%), and others (26.3%). These results suggest that more attention should be directed to genetic counselling.

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