Literature DB >> 31040149

Multicoloured lenticular opacities in a case of cerulean cataract.

Devesh Kumawat1, Navarosh Jayaraman1, Pranita Sahay1, Parijat Chandra1.   

Abstract

Entities:  

Keywords:  cataract; pediatrics

Mesh：

Year:  2019        PMID： 31040149      PMCID： PMC6506086          DOI： 10.1136/bcr-2019-230167

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN： 1757-790X


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  5 in total

1.  Cerulean cataract.

Authors:  J Ram; A Singh
Journal:  QJM       Date:  2019-09-01

2.  Cerulean Cataract.

Authors:  Lorraine M Provencher; Brice Critser; A Tim Johnson
Journal:  JAMA Ophthalmol       Date:  2018-12-13       Impact factor: 7.389

3.  Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2.

Authors:  M Litt; R Carrero-Valenzuela; D M LaMorticella; D W Schultz; T N Mitchell; P Kramer; I H Maumenee
Journal:  Hum Mol Genet       Date:  1997-05       Impact factor: 6.150

4.  A progressive early onset cataract gene maps to human chromosome 17q24.

Authors:  M M Armitage; J D Kivlin; R E Ferrell
Journal:  Nat Genet       Date:  1995-01       Impact factor: 38.330

5.  Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP.

Authors:  Xueshan Xiao; Wei Li; Panfeng Wang; Lin Li; Shiqiang Li; Xiaoyun Jia; Wenmin Sun; Xiangming Guo; Qingjiong Zhang
Journal:  Mol Vis       Date:  2011-07-26       Impact factor: 2.367
  5 in total

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