An aetiological study on 6 to 14 years-old children with severe visual handicap in Hungary.

Acta paediatrica Hungarica Pub Date : 1991-01-01
A Czeizel, E Törzs, L G Diaz, J Kovács, G Szabó, M Vitéz
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Abstract

A population-based aetiological study was carried out on 6 to 14 years-old severely visually handicapped children in Hungary. Of the 547 recorded cases 491 (90%) were included in the analysis. Eleven aetiological groups were separated: isolated cataracts (16.7%), congenital abnormalities of the eye (15.1%), high myopia +/- retinal detachment and other cases (13.4%), retinopathy of premature (11.0%), choroidoretinal degenerations (10.0%), syndromes (9.6%), nystagmus and/or hypermetropia (9.0%), isolated and complicated optic atrophy (6.7%), postnatal causes (4.9%), retinoblastoma (1.8%), prenatal causes (1.8%). A significantly higher rate of previous induced abortions was found in the group of retinopathy of premature. Perinatal damage syndrome and Mendelian monogenic defects are the two most common aetiological categories in the origin of severe visual handicaps in Hungary.

匈牙利6 ~ 14岁严重视力障碍儿童的病因学研究。
对匈牙利6至14岁严重视障儿童进行了一项以人群为基础的病因学研究。在547例记录病例中,有491例(90%)纳入分析。11个病因组分别为:孤立性白内障(16.7%)、先天性眼异常(15.1%)、高度近视+/-视网膜脱离等(13.4%)、早产儿视网膜病变(11.0%)、脉络膜视网膜变性(10.0%)、综合征(9.6%)、眼球震颤和/或远视(9.0%)、孤立性及复杂性视神经萎缩(6.7%)、产后原因(4.9%)、视网膜母细胞瘤(1.8%)、产前原因(1.8%)。早产儿视网膜病变组既往人工流产率明显增高。围产期损害综合征和孟德尔单基因缺陷是两种最常见的病因分类在匈牙利严重视力障碍的起源。
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