Granular Corneal Dystrophy Type II

A paradigm shift has been observed in the classification of Granular corneal dystrophies (GCD). GCD is a bilateral, progressive, genetically determined and non-inflammatory disease limited to the cornea that has an autosomal dominant mode of inheritance. A 28 year old young male presented to us with...

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Main Authors: Siddharth Madan, Sarita Beri
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-10-01
Series:Delhi Journal of Ophthalmology
Subjects:
Online Access:https://journals.lww.com/10.7869/djo.605
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author Siddharth Madan
Sarita Beri
author_facet Siddharth Madan
Sarita Beri
author_sort Siddharth Madan
collection DOAJ
description A paradigm shift has been observed in the classification of Granular corneal dystrophies (GCD). GCD is a bilateral, progressive, genetically determined and non-inflammatory disease limited to the cornea that has an autosomal dominant mode of inheritance. A 28 year old young male presented to us without any visual complaints. The examination of his cornea revealed the presence of diffuse linear, multiple round to granular, bread crumb like and stellate opacities extending from the sub-epithelium migrating down till the deep stroma, the classical clinical features of a heterozygous phenotypic variant of GCD type II. It progresses slowly and majority of the affected patients maintain a stable vision. Since this patient was asymptomatic therefore a complete ophthalmic examination in routine cases presenting to the oupatient clinics is indispensible. Various management options exist but a definitive treatment option is lacking.
format Article
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institution Kabale University
issn 0972-0200
2454-2784
language English
publishDate 2020-10-01
publisher Wolters Kluwer Medknow Publications
record_format Article
series Delhi Journal of Ophthalmology
spelling doaj-art-c787ced69263408abcac9d6d73b69b382025-08-20T03:52:29ZengWolters Kluwer Medknow PublicationsDelhi Journal of Ophthalmology0972-02002454-27842020-10-013129910210.7869/djo.605Granular Corneal Dystrophy Type IISiddharth MadanSarita BeriA paradigm shift has been observed in the classification of Granular corneal dystrophies (GCD). GCD is a bilateral, progressive, genetically determined and non-inflammatory disease limited to the cornea that has an autosomal dominant mode of inheritance. A 28 year old young male presented to us without any visual complaints. The examination of his cornea revealed the presence of diffuse linear, multiple round to granular, bread crumb like and stellate opacities extending from the sub-epithelium migrating down till the deep stroma, the classical clinical features of a heterozygous phenotypic variant of GCD type II. It progresses slowly and majority of the affected patients maintain a stable vision. Since this patient was asymptomatic therefore a complete ophthalmic examination in routine cases presenting to the oupatient clinics is indispensible. Various management options exist but a definitive treatment option is lacking.https://journals.lww.com/10.7869/djo.605granular corneal dystrophy type iicorneal dystrophy
spellingShingle Siddharth Madan
Sarita Beri
Granular Corneal Dystrophy Type II
Delhi Journal of Ophthalmology
granular corneal dystrophy type ii
corneal dystrophy
title Granular Corneal Dystrophy Type II
title_full Granular Corneal Dystrophy Type II
title_fullStr Granular Corneal Dystrophy Type II
title_full_unstemmed Granular Corneal Dystrophy Type II
title_short Granular Corneal Dystrophy Type II
title_sort granular corneal dystrophy type ii
topic granular corneal dystrophy type ii
corneal dystrophy
url https://journals.lww.com/10.7869/djo.605
work_keys_str_mv AT siddharthmadan granularcornealdystrophytypeii
AT saritaberi granularcornealdystrophytypeii