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匈牙利6至14岁严重视力障碍儿童的病因学研究。

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

作者信息

Czeizel A, Törzs E, Diaz L G, Kovács J, Szabó G, Vitéz M

机构信息

Department of Human Genetics and Teratology, WHO Collaborating Centre for the Community Control of Hereditary Diseases, Budapest, Hungary.

出版信息

Acta Paediatr Hung. 1991;31(3):365-77.

PMID:1742050
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.

摘要

在匈牙利,针对6至14岁的严重视力障碍儿童开展了一项基于人群的病因学研究。在记录的547例病例中,491例(90%)纳入分析。病因分为11组:单纯性白内障(16.7%)、眼部先天性异常(15.1%)、高度近视伴或不伴视网膜脱离及其他病例(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%)、单纯性和复杂性视神经萎缩(6.7%)、产后病因(4.9%)、视网膜母细胞瘤(1.8%)、产前病因(1.8%)。在早产儿视网膜病变组中,既往人工流产率显著更高。围产期损伤综合征和孟德尔单基因缺陷是匈牙利严重视力障碍病因中最常见的两类。

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