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Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes

PURPOSE: To investigate the phenotypic variability of patients bearing the heterozygous R124H mutation in the TGFBI (transforming growth factor-beta-induced) gene that causes granular corneal dystrophy type 2 (GCD2). METHODS: We describe the phenotypic range of GCD2 heterozygotes for the common R124...

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Autores principales: Han, Kyung Eun, Choi, Seung-il, Chung, Woo Suk, Jung, Se Hwan, Katsanis, Nicholas, Kim, Tae-im, Kim, Eung Kweon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2012
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398492/
https://www.ncbi.nlm.nih.gov/pubmed/22815629
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author Han, Kyung Eun
Choi, Seung-il
Chung, Woo Suk
Jung, Se Hwan
Katsanis, Nicholas
Kim, Tae-im
Kim, Eung Kweon
author_facet Han, Kyung Eun
Choi, Seung-il
Chung, Woo Suk
Jung, Se Hwan
Katsanis, Nicholas
Kim, Tae-im
Kim, Eung Kweon
author_sort Han, Kyung Eun
collection PubMed
description PURPOSE: To investigate the phenotypic variability of patients bearing the heterozygous R124H mutation in the TGFBI (transforming growth factor-beta-induced) gene that causes granular corneal dystrophy type 2 (GCD2). METHODS: We describe the phenotypic range of GCD2 heterozygotes for the common R124H mutation in TGFBI; seven with an extremely mild phenotype and six with an extremely severe phenotype. Detailed slit-lamp photographs of these patients were generated. All patients had no history of ocular surgery and were diagnosed as being heterozygous for GCD2 by DNA analysis from peripheral blood. Expression levels of transforming growth factor-beta-induced protein (TGFBIp) were compared among cultured corneal fibroblasts from ten normal donors. RESULTS: We report profound differences in the severity of the phenotype across our case series. Two patients with a mild phenotype were diagnosed as unaffected at presentation; however follow-up examinations revealed granular deposits. Importantly, we also observed familial clustering of phenotypic variance; five patients from two families with a mild phenotype showed a similarly mild phenotype within family members. Similarly, six patients from two families with severe phenotypes showed corneal deposits with similar patterns and severity within each distinct family, but distinct patterns between families. TGFBIp expressions from different donor derived cultured corneal fibroblasts were different between one another. CONCLUSIONS: GCD2 heterozygotes have extremely varied phenotypes between individual patients. However phenotypes were broadly consistent within families, suggesting that the observed variable expressivity might be regulated by other genetic factors that could influence the abundance of TGFBIp or the function of the pathway. From a clinical perspective, our data also highlighted that genetic analysis and meticulous slit-lamp examination in both eyes at multiple time intervals is necessary.
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spelling pubmed-33984922012-07-19 Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes Han, Kyung Eun Choi, Seung-il Chung, Woo Suk Jung, Se Hwan Katsanis, Nicholas Kim, Tae-im Kim, Eung Kweon Mol Vis Research Article PURPOSE: To investigate the phenotypic variability of patients bearing the heterozygous R124H mutation in the TGFBI (transforming growth factor-beta-induced) gene that causes granular corneal dystrophy type 2 (GCD2). METHODS: We describe the phenotypic range of GCD2 heterozygotes for the common R124H mutation in TGFBI; seven with an extremely mild phenotype and six with an extremely severe phenotype. Detailed slit-lamp photographs of these patients were generated. All patients had no history of ocular surgery and were diagnosed as being heterozygous for GCD2 by DNA analysis from peripheral blood. Expression levels of transforming growth factor-beta-induced protein (TGFBIp) were compared among cultured corneal fibroblasts from ten normal donors. RESULTS: We report profound differences in the severity of the phenotype across our case series. Two patients with a mild phenotype were diagnosed as unaffected at presentation; however follow-up examinations revealed granular deposits. Importantly, we also observed familial clustering of phenotypic variance; five patients from two families with a mild phenotype showed a similarly mild phenotype within family members. Similarly, six patients from two families with severe phenotypes showed corneal deposits with similar patterns and severity within each distinct family, but distinct patterns between families. TGFBIp expressions from different donor derived cultured corneal fibroblasts were different between one another. CONCLUSIONS: GCD2 heterozygotes have extremely varied phenotypes between individual patients. However phenotypes were broadly consistent within families, suggesting that the observed variable expressivity might be regulated by other genetic factors that could influence the abundance of TGFBIp or the function of the pathway. From a clinical perspective, our data also highlighted that genetic analysis and meticulous slit-lamp examination in both eyes at multiple time intervals is necessary. Molecular Vision 2012-06-27 /pmc/articles/PMC3398492/ /pubmed/22815629 Text en Copyright © 2012 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Han, Kyung Eun
Choi, Seung-il
Chung, Woo Suk
Jung, Se Hwan
Katsanis, Nicholas
Kim, Tae-im
Kim, Eung Kweon
Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes
title Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes
title_full Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes
title_fullStr Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes
title_full_unstemmed Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes
title_short Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes
title_sort extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398492/
https://www.ncbi.nlm.nih.gov/pubmed/22815629
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