Literature DB >> 16671898

2005 Gregg Lecture: Congenital cataract--from rubella to genetics.

David A Mackey1.   

Abstract

On the 65th anniversary of Gregg's observation "Congenital cataract following German measles in the mother", rubella has retired as the leading cause of congenital cataract, from 87% of Gregg's cohort to less than 3% over the last 25 years and almost zero now in Australia and other developed countries. However, people must keep vigilance in maintaining immunization rates and encourage immunization in developing countries. At least one-fifth of congenital cataract is familial. Understanding the genetics of familial cataract will lead to better treatment of congenital as well as age-related cataract.

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Year:  2006        PMID: 16671898     DOI: 10.1111/j.1442-9071.2006.01194.x

Source DB:  PubMed          Journal:  Clin Exp Ophthalmol        ISSN: 1442-6404            Impact factor:   4.207


  3 in total

1.  A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.

Authors:  Li-Yun Zhang; Bo Gong; Jian-Ping Tong; Dorothy Shu-Ping Fan; Sylvia Wai-Yee Chiang; Dinghua Lou; Dennis Shun-Chiu Lam; Gary Hin-Fai Yam; Chi-Pui Pang
Journal:  Mol Vis       Date:  2009-08-06       Impact factor: 2.367

2.  Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family.

Authors:  D A Mackey; A W Hewitt; J B Ruddle; B Vote; R G Buttery; C Toomes; R Metlapally; Y J Li; K N Tran-Viet; F Malecaze; P Calvas; T Rosenberg; J A Guggenheim; T L Young
Journal:  Mol Vis       Date:  2011-08-10       Impact factor: 2.367

Review 3.  X-linked inheritances recessive of congenital nystagmus and autosomal dominant inheritances of congenital cataracts coexist in a Chinese family: a case report and literature review.

Authors:  Naihong Yan; Lirong Xiao; Chen Hou; Bo Guo; Wei Fan; Yingping Deng; Ke Ma
Journal:  BMC Med Genet       Date:  2019-03-19       Impact factor: 2.103

  3 in total

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