Literature DB >> 33513810

Genotypic Homogeneity in Distinctive Transforming Growth Factor-Beta Induced (TGFBI) Protein Phenotypes.

Sang Beom Han1,2, Venkatraman Anandalakshmi3, Chee Wai Wong3,4, Si Rui Ng3,4, Jodhbir S Mehta4,5.   

Abstract

Background: To evaluate the distribution of the transforming growth factor-beta induced (TGFBI) corneal dystrophies in a multi-ethnic population in Singapore, and to present the different phenotypes with the same genotype.
Methods: This study included 32 patients. Slit lamp biomicroscopy was performed for each patient to determine the disease phenotype. Genomic DNA was extracted from the blood samples and the 17 exons of the TGFBI gene were amplified by PCR and sequenced bi-directionally for genotype analysis.
Results: Regarding phenotypes, the study patients comprised 11 (34.4%; 8 with R555W and 3 with R124H mutation) patients with granular corneal dystrophy type 1 (GCD1), 6 (18.8%; 5 with R124H and 1 with R124C mutation) patients with GCD2, 13 (40.6%; 7 with R124C, 2 with H626R, 2 with L550P, 1 with A620D and 1 with H572R) patients with lattice corneal dystrophy (LCD) and 2 (6.3%; 1 with R124L and 1 with R124C) patients with Reis-Bückler corneal dystrophy. Regarding genotype, R124H mutation was associated with GCD2 (5 cases; 62.5%) and GCD1 (3 cases; 37.5%). R124C mutation was associated with LCD (7 cases; 87.5%) and GCD2 (1 case; 12.5%). All the 8 cases (100%) of R555W mutation were associated with GCD1. Conclusions: Although the association between genotype and phenotype was good in most cases (65.7%; 21 of 32 patients), genotype/phenotype discrepancy was observed in a significant number.

Entities:  

Keywords:  TGFBI; aggregation disorders; corneal dystrophy; granular corneal dystrophy; lattice corneal dystrophy; transforming growth factor beta induced protein

Mesh:

Substances:

Year:  2021        PMID: 33513810      PMCID: PMC7866065          DOI: 10.3390/ijms22031230

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  44 in total

1.  Prevalence of granular corneal dystrophy type 2 (Avellino corneal dystrophy) in the Korean population.

Authors:  Jae Hwan Lee; Stephen M Cristol; Woon Cho Kim; Eui Sang Chung; Hungwon Tchah; Man Soo Kim; Chung Mo Nam; Hyun-Soo Cho; Eung Kweon Kim
Journal:  Ophthalmic Epidemiol       Date:  2010-06       Impact factor: 1.648

2.  Mutation update: TGFBI pathogenic and likely pathogenic variants in corneal dystrophies.

Authors:  Valeria Kheir; Vianney Cortés-González; Juan C Zenteno; Daniel F Schorderet
Journal:  Hum Mutat       Date:  2019-03-28       Impact factor: 4.878

3.  BIGH3 mutation spectrum in corneal dystrophies.

Authors:  Francis L Munier; Beatrice E Frueh; Philippe Othenin-Girard; Sylvie Uffer; Pascal Cousin; Ming X Wang; Elise Héon; Graeme C M Black; Maria A Blasi; Emilio Balestrazzi; Birgit Lorenz; Rafael Escoto; Rafael Barraquer; Maria Hoeltzenbein; Balder Gloor; Maurizio Fossarello; Arun D Singh; Yvan Arsenijevic; Léonidas Zografos; Daniel F Schorderet
Journal:  Invest Ophthalmol Vis Sci       Date:  2002-04       Impact factor: 4.799

4.  TGFBI gene mutations in Brazilian patients with corneal dystrophy.

Authors:  H P Solari; M P Ventura; A B A Perez; J M F Sallum; M N Burnier; R Belfort
Journal:  Eye (Lond)       Date:  2006-01-27       Impact factor: 3.775

5.  TGFBI gene mutation analysis in a Chinese pedigree of Reis-Bücklers corneal dystrophy.

Authors:  Ke Ma; Guo Liu; Yin Yang; Man Yu; Ruifang Sui; Wenhan Yu; Xiaoming Chen; Yinping Deng; Naihong Yan; Guiqun Cao; Xuyang Liu
Journal:  Mol Vis       Date:  2010-03-31       Impact factor: 2.367

Review 6.  Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature.

Authors:  Juhua Yang; Xiaoli Han; Dinggou Huang; Lin Yu; Yihua Zhu; Yi Tong; Binliang Zhu; Chuanbao Li; Mingshe Weng; Xu Ma
Journal:  Mol Vis       Date:  2010-06-30       Impact factor: 2.367

7.  Genotype-Phenotype Correlation for TGFBI Corneal Dystrophies Identifies p.(G623D) as a Novel Cause of Epithelial Basement Membrane Dystrophy.

Authors:  Cerys J Evans; Alice E Davidson; Nicole Carnt; Karla E Rojas López; Neyme Veli; Caroline M Thaung; Stephen J Tuft; Alison J Hardcastle
Journal:  Invest Ophthalmol Vis Sci       Date:  2016-10-01       Impact factor: 4.799

8.  Genotype-phenotype correlation of TGFBI corneal dystrophies in Polish patients.

Authors:  Anna K Nowińska; Edward Wylegala; Dominika A Janiszewska; Dariusz Dobrowolski; Pasquale Aragona; Anna M Roszkowska; Domenico Puzzolo
Journal:  Mol Vis       Date:  2011-08-30       Impact factor: 2.367

9.  Phenotype-genotype correlations in patients with TGFBI-linked corneal dystrophies in Taiwan.

Authors:  Yu-Chih Hou; I-Jong Wang; Cheng-Hsiang Hsiao; Wei-Li Chen; Fung-Rong Hu
Journal:  Mol Vis       Date:  2012-02-07       Impact factor: 2.367

10.  Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes.

Authors:  Kyung Eun Han; Seung-il Choi; Woo Suk Chung; Se Hwan Jung; Nicholas Katsanis; Tae-im Kim; Eung Kweon Kim
Journal:  Mol Vis       Date:  2012-06-27       Impact factor: 2.367

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