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Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child
A 14-year-old male presented with decreased vision. Slit lamp examination indicated multiple anterior corneal stromal opacities with clear intervening spaces accompanied with superficial subepithelial lines arranged in a quasi-whorl-like fashion bilateral with greater prominence in the right eye. Co...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968150/ https://www.ncbi.nlm.nih.gov/pubmed/27555713 http://dx.doi.org/10.4103/0974-9233.186151 |
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author | Dangra, Kavita Lohiya Das, Manoranjan Periasamy, Sundersan Prajna, N. Venkatesh |
author_facet | Dangra, Kavita Lohiya Das, Manoranjan Periasamy, Sundersan Prajna, N. Venkatesh |
author_sort | Dangra, Kavita Lohiya |
collection | PubMed |
description | A 14-year-old male presented with decreased vision. Slit lamp examination indicated multiple anterior corneal stromal opacities with clear intervening spaces accompanied with superficial subepithelial lines arranged in a quasi-whorl-like fashion bilateral with greater prominence in the right eye. Corneal steepening associated with thinning was noted only in the right eye. Genetic analysis confirmed a mutation suggestive of granular corneal dystrophy. Here, we describe a rare case of an atypical granular dystrophy associated with unilateral keratoconus in a male child. |
format | Online Article Text |
id | pubmed-4968150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49681502016-08-23 Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child Dangra, Kavita Lohiya Das, Manoranjan Periasamy, Sundersan Prajna, N. Venkatesh Middle East Afr J Ophthalmol Case Report A 14-year-old male presented with decreased vision. Slit lamp examination indicated multiple anterior corneal stromal opacities with clear intervening spaces accompanied with superficial subepithelial lines arranged in a quasi-whorl-like fashion bilateral with greater prominence in the right eye. Corneal steepening associated with thinning was noted only in the right eye. Genetic analysis confirmed a mutation suggestive of granular corneal dystrophy. Here, we describe a rare case of an atypical granular dystrophy associated with unilateral keratoconus in a male child. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4968150/ /pubmed/27555713 http://dx.doi.org/10.4103/0974-9233.186151 Text en Copyright: © Middle East African Journal of Ophthalmology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Dangra, Kavita Lohiya Das, Manoranjan Periasamy, Sundersan Prajna, N. Venkatesh Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child |
title | Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child |
title_full | Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child |
title_fullStr | Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child |
title_full_unstemmed | Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child |
title_short | Bilateral Atypical Granular Corneal Dystrophy Associated with Unilateral Keratoconus in a Male Child |
title_sort | bilateral atypical granular corneal dystrophy associated with unilateral keratoconus in a male child |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968150/ https://www.ncbi.nlm.nih.gov/pubmed/27555713 http://dx.doi.org/10.4103/0974-9233.186151 |
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