Literature DB >> 16288201

A new congenital nuclear cataract caused by a missense mutation in the gammaD-crystallin gene (CRYGD) in a Chinese family.

Jingzhi Gu1, Yanhua Qi, Li Wang, Jin Wang, Lisong Shi, Hui Lin, Xiang Li, Hong Su, Shangzhi Huang.   

Abstract

PURPOSE: To identify genetic defects associated with nuclear golden crystal autosomal dominant congenital cataract (ADCC) in a Chinese pedigree in the north of China.
METHODS: Clinical data were collected and the phenotype of the affected members in this family was recorded by slit lamp photography. Genomic DNA was isolated from peripheral blood. Linkage analyses excluded all known loci except that in 2q33-q35. Mutation analysis of CRYGs was carried by direct sequencing of the PCR products.
RESULTS: Sequencing of the coding regions of CRYGA, CRYGB, CRYGC, and CRYGD showed the presence of a heterozygous C>A transversion at nt109 of the coding sequence (R36S) in exon 2 of CRYGD, which co-segregated with the affected members.
CONCLUSIONS: The R36S mutation in CRYGD identified in this Chinese family caused a nuclear golden crystal cataract phenotype not described before. This finding is an additional indication that there may be phenotypic heterogeneity of cataract, especially in different races.

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Year:  2005        PMID: 16288201

Source DB:  PubMed          Journal:  Mol Vis        ISSN: 1090-0535            Impact factor:   2.367


  8 in total

Review 1.  Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.

Authors:  Olga Messina-Baas; Sergio A Cuevas-Covarrubias
Journal:  Mol Syndromol       Date:  2017-02-07

2.  A novel human CRYGD mutation in a juvenile autosomal dominant cataract.

Authors:  Mascarenhas Roshan; Pai H Vijaya; G Rao Lavanya; Prasada K Shama; S T Santhiya; Jochen Graw; P M Gopinath; K Satyamoorthy
Journal:  Mol Vis       Date:  2010-05-22       Impact factor: 2.367

3.  Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state.

Authors:  Olga V Plotnikova; Fyodor A Kondrashov; Peter K Vlasov; Anastasia P Grigorenko; Evgeny K Ginter; Evgeny I Rogaev
Journal:  Am J Hum Genet       Date:  2007-05-16       Impact factor: 11.025

4.  A novel mutation in γD-crystallin associated with autosomal dominant congenital cataract in a Chinese family.

Authors:  Li Wang; Xueli Chen; Yi Lu; Jihong Wu; Boqi Yang; Xinghuai Sun
Journal:  Mol Vis       Date:  2011-03-26       Impact factor: 2.367

5.  The congenital cataract-linked G61C mutation destabilizes γD-crystallin and promotes non-native aggregation.

Authors:  Wang Zhang; Hong-Chen Cai; Fei-Feng Li; Yi-Bo Xi; Xu Ma; Yong-Bin Yan
Journal:  PLoS One       Date:  2011-05-31       Impact factor: 3.240

6.  Crystalline cataract caused by a heterozygous missense mutation in γD-crystallin (CRYGD).

Authors:  Deborah K VanderVeen; Caroline Andrews; Bharti R Nihalani; Elizabeth C Engle
Journal:  Mol Vis       Date:  2011-12-20       Impact factor: 2.367

7.  Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts.

Authors:  Feifeng Li; Shuzhen Wang; Chang Gao; Shiguo Liu; Baojian Zhao; Meng Zhang; Shangzhi Huang; Siquan Zhu; Xu Ma
Journal:  Mol Vis       Date:  2008-03-04       Impact factor: 2.367

8.  A nonsense mutation of γD-crystallin associated with congenital nuclear and posterior polar cataract in a Chinese family.

Authors:  Yi Zhai; Jinyu Li; Yanan Zhu; Yan Xia; Wei Wang; Yinhui Yu; Ke Yao
Journal:  Int J Med Sci       Date:  2014-01-05       Impact factor: 3.738

  8 in total

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