• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Congenital ocular blindness in children, 1945 to 1984.

作者信息

Robinson G C, Jan J E, Kinnis C

机构信息

Department of Pediatrics, Faculty of Medicine, B.C. Children's Hospital, Vancouver, Canada.

出版信息

Am J Dis Child. 1987 Dec;141(12):1321-4. doi: 10.1001/archpedi.1987.04460120087041.

DOI:10.1001/archpedi.1987.04460120087041
PMID:3687875
Abstract

A total of 676 children born in British Columbia with congenital ocular blindness during the years 1945 through 1984 were studied. The birth prevalence rate of congenital blindness has decreased from eight per 10,000 live births in the late 1940s to three per 10,000 live births. Retinopathy of prematurity was replaced by genetic ocular disorders as the leading cause of congenital blindness, although the former is reemerging. The rate of congenital rubella infection also declined. There has been a significant increase in the rate of births with optic nerve lesions during the past 15 years, while the rate of births with lesions of the lens fell, reflecting the decline in the rate of maternal rubella infection. There are fewer children with congenital ocular legal blindness who have no light perception today, and they also have fewer associated handicaps.

摘要

相似文献

1
Congenital ocular blindness in children, 1945 to 1984.
Am J Dis Child. 1987 Dec;141(12):1321-4. doi: 10.1001/archpedi.1987.04460120087041.
2
A study of congenital blindness in British Columbia. Epidemiological findings.不列颠哥伦比亚省先天性失明研究。流行病学调查结果。
Can J Ophthalmol. 1969 Apr;4(2):152-62.
3
Retinopathy of prematurity-induced blindness: birth weight-specific survival and the new epidemic.早产儿视网膜病变导致的失明:特定出生体重的存活率与新的流行情况
Pediatrics. 1990 Sep;86(3):405-12.
4
A study of congenital blindness in British Columbia: methodology and medical findings.不列颠哥伦比亚省先天性失明研究:方法与医学发现
Can Med Assoc J. 1968 Nov 2;99(17):831-6.
5
Acquired ocular visual impairment in children. 1960-1989.儿童获得性视力损害。1960 - 1989年。
Am J Dis Child. 1993 Mar;147(3):325-8. doi: 10.1001/archpedi.1993.02160270087028.
6
Retinopathy of prematurity: a new epidemic?早产儿视网膜病变:一种新的流行病?
Pediatrics. 1989 Apr;83(4):486-92.
7
Changing pattern of retinopathy of prematurity: a 37-year clinic experience.
Pediatrics. 1988 Sep;82(3):344-9.
8
Childhood blindness and visual loss: an assessment at two institutions including a "new" cause.儿童失明和视力丧失:在两家机构进行的评估,包括一种“新”病因。
Trans Am Ophthalmol Soc. 1999;97:653-96.
9
Children with blindness - major causes, developmental outcomes and implications for habilitation and educational support: a two-decade, Swedish population-based study.失明儿童——主要病因、发育结果以及对康复和教育支持的影响:一项为期二十年的瑞典基于人群的研究。
Acta Ophthalmol. 2018 May;96(3):295-300. doi: 10.1111/aos.13631. Epub 2017 Nov 23.
10
The ocular manifestations of congenital infection: a study of the early effect and long-term outcome of maternally transmitted rubella and toxoplasmosis.先天性感染的眼部表现:一项关于母婴传播风疹和弓形虫病早期影响及长期结局的研究。
Trans Am Ophthalmol Soc. 1998;96:813-79.

引用本文的文献

1
A novel modulator of IL-6R prevents inflammation-induced preterm birth and improves newborn outcome.一种新型白细胞介素-6受体调节剂可预防炎症诱导的早产并改善新生儿结局。
EMBO Mol Med. 2025 Jul 3. doi: 10.1038/s44321-025-00257-9.
2
Pharmacokinetics of Monoclonal Antibody and Antibody Fragments in the Mouse Eye Following Systemic Administration.全身性给药后小鼠眼内单克隆抗体和抗体片段的药代动力学。
AAPS J. 2021 Nov 8;23(6):116. doi: 10.1208/s12248-021-00647-0.
3
Corrigendum: Base Rates, Blindness, and Schizophrenia.勘误:基础概率、失明与精神分裂症。
Front Psychol. 2021 Sep 21;12:732333. doi: 10.3389/fpsyg.2021.732333. eCollection 2021.
4
Modeling congenital cataract in vitro using patient-specific induced pluripotent stem cells.使用患者特异性诱导多能干细胞在体外模拟先天性白内障。
NPJ Regen Med. 2021 Oct 1;6(1):60. doi: 10.1038/s41536-021-00171-x.
5
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene.西伯利亚雅库特人群体性常染色体隐性白内障(CTRCT18):FYCO1 基因中的新型创始变体。
Eur J Hum Genet. 2021 Jun;29(6):965-976. doi: 10.1038/s41431-021-00833-w. Epub 2021 Mar 25.
6
Mutations in identified in families with congenital cataracts.在先天性白内障的家族中发现了 突变。
Mol Vis. 2020 Apr 28;26:334-344. eCollection 2020.
7
Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family.常染色体隐性遗传性先天性白内障一家系与 HSF4 基因相关
PLoS One. 2019 Dec 9;14(12):e0225010. doi: 10.1371/journal.pone.0225010. eCollection 2019.
8
Novel mutations associated with autosomal-dominant congenital cataract identified in Chinese families.在中国家庭中鉴定出与常染色体显性先天性白内障相关的新型突变。
Exp Ther Med. 2019 Oct;18(4):2701-2710. doi: 10.3892/etm.2019.7865. Epub 2019 Aug 8.
9
Proteome Profiling of Developing Murine Lens Through Mass Spectrometry.通过质谱法对发育中的鼠晶状体进行蛋白质组学分析。
Invest Ophthalmol Vis Sci. 2018 Jan 1;59(1):100-107. doi: 10.1167/iovs.17-21601.
10
Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening.通过纯合性筛查对患有常染色体隐性先天性白内障的巴基斯坦家庭进行分子遗传学分析。
Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2207-2217. doi: 10.1167/iovs.17-21469.