Literature DB >> 20090209

Genetics of corneal endothelial dystrophies.

Chitra Kannabiran1.   

Abstract

The corneal endothelium maintains the level of hydration in the cornea. Dysfunction of the endothelium results in excess accumulation of water in the corneal stroma, leading to swelling of the stroma and loss of transparency. There are four different corneal endothelial dystrophies that are hereditary, progressive, non-inflammatory disorders involving dysfunction of the corneal endothelium. Each of the endothelial dystrophies is genetically heterogeneous with different modes of transmission and/or different genes involved in each subtype. Genes responsible for disease have been identified for only a subset of corneal endothelial dystrophies. Knowledge of genes involved and their function in the corneal endothelium can aid understanding the pathogenesis of the disorder as well as reveal pathways that are important for normal functioning of the endothelium.

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Year:  2009        PMID: 20090209     DOI: 10.1007/s12041-009-0067-1

Source DB:  PubMed          Journal:  J Genet        ISSN: 0022-1333            Impact factor:   1.166


  64 in total

1.  Corneal dystrophies among patients undergoing keratoplasty in Saudi Arabia.

Authors:  M F al Faran; K F Tabbara
Journal:  Cornea       Date:  1991-01       Impact factor: 2.651

2.  No pathogenic mutations identified in the COL8A2 gene or four positional candidate genes in patients with posterior polymorphous corneal dystrophy.

Authors:  Vivek S Yellore; Sylvia A Rayner; Leslie Emmert-Buck; Geoffrey C Tabin; Irving Raber; Sadeer B Hannush; R Doyle Stulting; Kapil Sampat; Rominder Momi; Alexandre H Principe; Anthony J Aldave
Journal:  Invest Ophthalmol Vis Sci       Date:  2005-05       Impact factor: 4.799

3.  Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13pTel-13q12.13.

Authors:  Olof H Sundin; Albert S Jun; Karl W Broman; Sammy H Liu; Siobhan E Sheehan; Elizabeth C L Vito; Walter J Stark; John D Gottsch
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-01       Impact factor: 4.799

Review 4.  Trends in penetrating keratoplasty in the United States 1980-2005.

Authors:  Faris R Ghosheh; Federico A Cremona; Christopher J Rapuano; Elisabeth J Cohen; Brandon D Ayres; Kristin M Hammersmith; Irving M Raber; Peter R Laibson
Journal:  Int Ophthalmol       Date:  2008-06       Impact factor: 2.031

5.  Immunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patients.

Authors:  Katerina Jirsova; Stanislava Merjava; Radka Martincova; Rhian Gwilliam; Neil D Ebenezer; Petra Liskova; Martin Filipec
Journal:  Exp Eye Res       Date:  2006-12-15       Impact factor: 3.467

6.  Changing indications for penetrating keratoplasty in Taiwan from 1987 to 1999.

Authors:  W L Chen; F R Hu; I J Wang
Journal:  Cornea       Date:  2001-03       Impact factor: 2.651

7.  H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family.

Authors:  Sophie Valleix; Brigitte Nedelec; Florence Rigaudiere; Paul Dighiero; Yves Pouliquen; Gilles Renard; Jean-François Le Gargasson; Marc Delpech
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-01       Impact factor: 4.799

8.  Histopathological diagnosis of corneal button specimens: an epidemiological study.

Authors:  Katyanne D Godeiro; Anamaria B Coutinho; Patricia R Pereira; Bruno F Fernandes; Amanda Cassie; Miguel N Burnier
Journal:  Ophthalmic Epidemiol       Date:  2007 Mar-Apr       Impact factor: 1.648

9.  Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11.

Authors:  Arun Kumar; Soma Bhattacharjee; Durgappa Ravi Prakash; Chethan Sitarampur Sadanand
Journal:  Mol Vis       Date:  2007-01-16       Impact factor: 2.367

10.  DeltaEF1, a zinc finger and homeodomain transcription factor, is required for skeleton patterning in multiple lineages.

Authors:  T Takagi; H Moribe; H Kondoh; Y Higashi
Journal:  Development       Date:  1998-01       Impact factor: 6.868

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  6 in total

1.  Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process.

Authors:  Abraham Kuot; Alex W Hewitt; Kim Griggs; Sonja Klebe; Richard Mills; Vishal Jhanji; Jamie E Craig; Shiwani Sharma; Kathryn P Burdon
Journal:  Eur J Hum Genet       Date:  2012-01-11       Impact factor: 4.246

2.  Identification of novel molecular markers through transcriptomic analysis in human fetal and adult corneal endothelial cells.

Authors:  Yinyin Chen; Kevin Huang; Martin N Nakatsu; Zhigang Xue; Sophie X Deng; Guoping Fan
Journal:  Hum Mol Genet       Date:  2012-12-20       Impact factor: 6.150

3.  Abnormal regulation of extracellular matrix and adhesion molecules in corneas of patients with keratoconus.

Authors:  Yelena Bykhovskaya; Anastasia Gromova; Helen P Makarenkova; Yaron S Rabinowitz
Journal:  Int J Keratoconus Ectatic Corneal Dis       Date:  2016 May-Aug

Review 4.  Genetics in Keratoconus: where are we?

Authors:  Yelena Bykhovskaya; Benjamin Margines; Yaron S Rabinowitz
Journal:  Eye Vis (Lond)       Date:  2016-06-27

5.  TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases.

Authors:  Abraham Kuot; Alex W Hewitt; Grant R Snibson; Emmanuelle Souzeau; Richard Mills; Jamie E Craig; Kathryn P Burdon; Shiwani Sharma
Journal:  PLoS One       Date:  2017-08-23       Impact factor: 3.240

6.  Potential underlying genetic associations between keratoconus and diabetes mellitus.

Authors:  Kristin M Ates; Amy J Estes; Yutao Liu
Journal:  Adv Ophthalmol Pract Res       Date:  2021-09-04
  6 in total

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