Literature DB >> 20697279

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

Dhara A Patel1, Shu-Hong Chang, George J Harocopos, Smita C Vora, Diep Huu Thang, Andrew J W Huang.   

Abstract

PURPOSE: Both granular and lattice deposits are present in Avellino corneal dystrophy (ACD), primarily associated with the R124H mutation of transforming growth factor-β-induced (TGFBIp). We investigated the presence of these deposits in other TGFBI mutations and the use of Thioflavin-T (ThT), a fluorescent amyloid stain for characterizing corneal amyloid deposits.
METHODS: Surgical corneal specimens of 3 unrelated patients clinically diagnosed with ACD were studied. Corneal sections from normal individuals and patients with prior lattice corneal dystrophy (LCD) were used as controls. Histochemical studies were performed with Congo red and Masson trichrome stains, and fluorescent imaging with scanning laser confocal microscopy was performed for ThT and anti-TGFBIp antibody staining.
RESULTS: Clinical and histopathological findings supported the diagnoses of ACD in these 3 cases in whom granular deposits stained with Masson trichrome and lattice deposits stained with ThT and Congo red showed birefringence and dichroism as expected. However, genotyping revealed a heterozygous R124C mutation in each case. In addition to classical stromal deposits, unique subepithelial TGFBIp aggregates, which stain with neither ThT nor trichrome, were observed. In control LCD sections, stromal deposits were stained with ThT but not with trichrome, confirming lack of granular deposits.
CONCLUSIONS: Our results demonstrate that both granular and lattice corneal deposits can be associated with R124C mutation in addition to the more common R124H mutation. An additional feature of nonhyaline, nonamyloid, TGFBIp subepithelial deposits might substantiate the categorization of such cases as a variant form of ACD. This study further validates ThT staining for detection of amyloid TGFBIp deposits.

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Year:  2010        PMID: 20697279      PMCID: PMC2965268          DOI: 10.1097/ICO.0b013e3181d4f737

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


  47 in total

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2.  Heterogeneity in granular corneal dystrophy: identification of three causative mutations in the TGFBI (BIGH3) gene-lessons for corneal amyloidogenesis.

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

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4.  Allelic homogeneity in Avellino corneal dystrophy due to a founder effect.

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5.  Mutation screening of TGFBI in two Iranian Avellino corneal dystrophy pedigrees.

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6.  Homozygous granular corneal dystrophy type II (Avellino corneal dystrophy): natural history and progression after treatment.

Authors:  Jong Wook Moon; Sun Woong Kim; Tae-im Kim; Stephen M Cristol; Eui Sang Chung; Eung Kweon Kim
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  6 in total

1.  Unique TGFBI protein in lattice corneal dystrophy.

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2.  A unique TGFBI protein in granular corneal dystrophy types 1 and 2.

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Journal:  Curr Eye Res       Date:  2012-06-29       Impact factor: 2.424

3.  TGFBI, CHST6, and GSN gene analysis in Mexican patients with stromal corneal dystrophies.

Authors:  Johanna Gonzalez-Rodriguez; Arturo Ramirez-Miranda; Sergio E Hernandez-Da Mota; Juan C Zenteno
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4.  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
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5.  An Arg124His mutation in TGFBI associated to Avellino corneal dystrophy in a Chinese pedigree.

Authors:  Zhensheng Gu; Peiquan Zhao; Guang He; Chunling Wan; Gang Ma; Ling Yu; Juan Zhang; Guoyin Feng; Lin He; Linghan Gao
Journal:  Mol Vis       Date:  2011-12-13       Impact factor: 2.367

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

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Journal:  Int J Mol Sci       Date:  2021-01-27       Impact factor: 5.923

  6 in total

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