期刊文献+

Nature nurtures:lens regeneration,a breakthrough in ophthalmology 被引量:1

下载PDF
导出
摘要 Pediatric cataract is a major cause of treatable blindness worldwide(1,2).The prevalence of cataract in children has been estimated between 1-15/10,000 children(3).There are 200,000 children blind from cataract worldwide,and 20,000 to 40,000 children with developmental bilateral cataract are born each year(3).Pediatric cataracts are responsible for more than 1 million childhood blindness in Asia alone(3).Pediatric cataract blindness presents an enormous problem in terms of human morbidity,economic loss,and social burden.Despite the availability of meticulous surgery,cataract is still the leading cause of blindness worldwide in children(4).
机构地区 Advanced Eye Centre
出处 《Annals of Eye Science》 2017年第1期63-66,共4页 眼科学年鉴(英文)
关键词 RES BREAKTHROUGH ALONE
  • 相关文献

参考文献1

二级参考文献54

  • 1Khaliq S;Hameed A;Ismail M.A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani family,2002.
  • 2Hejtmancik JF.Congenital cataracts and their molecular genetics. Seminars in Cell and Developmental Biology . 2008
  • 3Haargaard B,Wohlfahrt J,Fledelius HC,Rosenberg T,Melbye M.A nationwideDanish study of 1027 cases of congenital/infantile cataracts: etiological and clinical classifications. Ophthalmology . 2004
  • 4West S.Epidemiology of cataract:accomplishments over 25 years and future directions. Ophthalmic Epidemiology . 2007
  • 5Linghan Gao,Wei Qin,Hao Cui,Guoyin Feng,Ping Liu,Weiqi Gao,Lin Ma,Pu Li,Lin He,Songbin Fu.A novel locus of coralliform cataract mapped to chromosome 2p24-pter[J]. Journal of Human Genetics . 2005 (6)
  • 6Gülistan Me?e,Eric Londin,Rickie Mui,Peter R. Brink,Thomas W. White.Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss[J]. Human Genetics . 2004 (3)
  • 7Hans Eiberg,Allan Meldgaard Lund,Mette Warburg,Thomas Rosenberg.Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36[J]. Human Genetics . 1995 (1)
  • 8Wang KJ,Li SS,Yun B,Ma WX,Jiang TG,Zhu SQ.A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family. Molecular Vision . 2011
  • 9Johar SR,Savalia NK,Vasavada AR,Gupta PD.Epidemiology based etiological study of pediatric cataract in western India. Indian Journal of Medical Sciences . 2004
  • 10Yang G,Xiong C,Li S,Wang Y,Zhao J.A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families. Molecular Vision . 2011

共引文献6

同被引文献3

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部