Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes

Kyung Eun Han, Seung il Choi, Woo Suk Chung, Se Hwan Jung, Nicholas Katsanis, Tae im Kim, Eung Kweon Kim

Research output: Contribution to journalArticle

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Abstract

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.

Original languageEnglish
Pages (from-to)1755-1762
Number of pages8
JournalMolecular vision
Volume18
Publication statusPublished - 2012 Jul 31

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Heterozygote
Phenotype
Transforming Growth Factor beta
Fibroblasts
Tissue Donors
Corneal dystrophy Avellino type
Mutation
Cluster Analysis
DNA

All Science Journal Classification (ASJC) codes

  • Ophthalmology

Cite this

Han, K. E., Choi, S. I., Chung, W. S., Jung, S. H., Katsanis, N., Kim, T. I., & Kim, E. K. (2012). Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes. Molecular vision, 18, 1755-1762.
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. In: Molecular vision. 2012 ; Vol. 18. pp. 1755-1762.
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abstract = "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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Han, KE, Choi, SI, Chung, WS, Jung, SH, Katsanis, N, Kim, TI & Kim, EK 2012, 'Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes', Molecular vision, vol. 18, pp. 1755-1762.

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.

In: Molecular vision, Vol. 18, 31.07.2012, p. 1755-1762.

Research output: Contribution to journalArticle

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AU - Choi, Seung il

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AU - Kim, Tae im

AU - Kim, Eung Kweon

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N2 - 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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Han KE, Choi SI, Chung WS, Jung SH, Katsanis N, Kim TI et al. Extremely varied phenotypes in granular corneal dystrophy type 2 heterozygotes. Molecular vision. 2012 Jul 31;18:1755-1762.