Literature DB >> 11189007

BIGH3 gene analysis in the differential diagnosis of corneal dystrophies.

A G Kocak-Altintas1, I Kocak-Midillioglu, A N Akarsu, S Duman.   

Abstract

PURPOSE: To identify the mutation in the keratoepithelin gene for proper diagnosis of granular corneal dystrophies.
METHODS: Four generations of a single family with corneal dystrophy were analyzed. Fourteen family members were examined and 11 were found to be affected by clinical evaluation. Genetic DNA was extracted from proband's leukocytes for molecular analysis. Exons 4 and 12 of the BIGH3 gene were amplified then directly sequenced.
RESULTS: The clinical appearance of corneas consisted of grayish white granules with sharp borders, fine dots, and radial lines in the superficial part of the central corneal stroma, which resembles granular and Avellino corneal dystrophies. Performing BIGH3 gene analysis, we observed a C-to-T transition at position 1710 (CGG to TGG) producing R555W mutation, which is a hot spot for granular corneal dystrophy.
CONCLUSION: Direct clinical examination may be insignificant in the proper diagnosis of corneal dystrophies, and molecular genetic approach may be required.

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Year:  2001        PMID: 11189007     DOI: 10.1097/00003226-200101000-00013

Source DB:  PubMed          Journal:  Cornea        ISSN: 0277-3740            Impact factor:   2.651


  7 in total

1.  Association of keratoconus and Avellino corneal dystrophy.

Authors:  S Igarashi; Y Makita; T Hikichi; F Mori; K Hanada; A Yoshida
Journal:  Br J Ophthalmol       Date:  2003-03       Impact factor: 4.638

2.  Granular and lattice deposits in corneal dystrophy caused by R124C mutation of TGFBIp.

Authors:  Dhara A Patel; Shu-Hong Chang; George J Harocopos; Smita C Vora; Diep Huu Thang; Andrew J W Huang
Journal:  Cornea       Date:  2010-11       Impact factor: 2.651

3.  Molecular genetics of Chinese families with TGFBI corneal dystrophies.

Authors:  Ting Zhang; Naihong Yan; Wenhan Yu; Yun Liu; Guo Liu; Xiaomei Wu; Jinxian Lian; Xuyang Liu
Journal:  Mol Vis       Date:  2011-02-04       Impact factor: 2.367

4.  De Novo L509P Mutation of the TGFBI Gene Associated with Slit-Lamp Findings of Lattice Corneal Dystrophy Type IIIA.

Authors:  Yong Woo Ji; Hyunmin Ahn; Kyoung-Jin Shin; Tae-Im Kim; Kyoung Yul Seo; R Doyle Stulting; Eung Kweon Kim
Journal:  J Clin Med       Date:  2022-05-28       Impact factor: 4.964

5.  Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6.

Authors:  Fulya Yaylacioglu Tuncay; Gülsüm Kayman Kurekci; Sezen Guntekin Ergun; Ozge Tugce Pasaoglu; Rustu Fikret Akata; Pervin Rukiye Dincer
Journal:  Mol Vis       Date:  2016-10-26       Impact factor: 2.367

6.  Mitomycin C induces apoptosis in cultured corneal fibroblasts derived from type II granular corneal dystrophy corneas.

Authors:  Tae-im Kim; Seung-il Choi; Hyung Keun Lee; Young Jae Cho; Eung Kweon Kim
Journal:  Mol Vis       Date:  2008-06-30       Impact factor: 2.367

7.  pH Induced Conformational Transitions in the Transforming Growth Factor β-Induced Protein (TGFβIp) Associated Corneal Dystrophy Mutants.

Authors:  Elavazhagan Murugan; Anandalakshmi Venkatraman; Zhou Lei; Victoria Mouvet; Rayne Rui Yi Lim; Nandhakumar Muruganantham; Eunice Goh; Gary Swee Lim Peh; Roger W Beuerman; Shyam S Chaurasia; Lakshminarayanan Rajamani; Jodhbir S Mehta
Journal:  Sci Rep       Date:  2016-03-31       Impact factor: 4.379

  7 in total

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