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Ophthalmic manifestations in Rothmund–Thomson syndrome: Case report and review of literature

A 24-year-old male patient presented to us with diminution of vision in both eyes with watering and photophobia for the past 8 years. General physical examination showed short stature and poikiloderma. Ocular findings include photophobia with reflex tearing, dry eye, cicatricial ectropion, symblepha...

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Autores principales: Chinmayee, J T, Meghana, G R, Prathiba, R K, Ramesh, T K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678305/
https://www.ncbi.nlm.nih.gov/pubmed/29044077
http://dx.doi.org/10.4103/ijo.IJO_89_17
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author Chinmayee, J T
Meghana, G R
Prathiba, R K
Ramesh, T K
author_facet Chinmayee, J T
Meghana, G R
Prathiba, R K
Ramesh, T K
author_sort Chinmayee, J T
collection PubMed
description A 24-year-old male patient presented to us with diminution of vision in both eyes with watering and photophobia for the past 8 years. General physical examination showed short stature and poikiloderma. Ocular findings include photophobia with reflex tearing, dry eye, cicatricial ectropion, symblepharon approaching pupillary area of cornea, and multiple superficial punctuate erosions on the cornea. Both eyelids showed scanty meibomian glands on infrared meibography. The rest of the anterior and posterior segment was normal. The patient was treated with topical lubricants which reduced photophobia and corneal erosions. He then underwent symblepharon release with buccal mucosal grafting, which improved ectropion. Patient improved symptomatically with reduction of photophobia and improvement in vision as well.
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spelling pubmed-56783052017-11-28 Ophthalmic manifestations in Rothmund–Thomson syndrome: Case report and review of literature Chinmayee, J T Meghana, G R Prathiba, R K Ramesh, T K Indian J Ophthalmol Brief Communications A 24-year-old male patient presented to us with diminution of vision in both eyes with watering and photophobia for the past 8 years. General physical examination showed short stature and poikiloderma. Ocular findings include photophobia with reflex tearing, dry eye, cicatricial ectropion, symblepharon approaching pupillary area of cornea, and multiple superficial punctuate erosions on the cornea. Both eyelids showed scanty meibomian glands on infrared meibography. The rest of the anterior and posterior segment was normal. The patient was treated with topical lubricants which reduced photophobia and corneal erosions. He then underwent symblepharon release with buccal mucosal grafting, which improved ectropion. Patient improved symptomatically with reduction of photophobia and improvement in vision as well. Medknow Publications & Media Pvt Ltd 2017-10 /pmc/articles/PMC5678305/ /pubmed/29044077 http://dx.doi.org/10.4103/ijo.IJO_89_17 Text en Copyright: © 2017 Indian 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 Brief Communications
Chinmayee, J T
Meghana, G R
Prathiba, R K
Ramesh, T K
Ophthalmic manifestations in Rothmund–Thomson syndrome: Case report and review of literature
title Ophthalmic manifestations in Rothmund–Thomson syndrome: Case report and review of literature
title_full Ophthalmic manifestations in Rothmund–Thomson syndrome: Case report and review of literature
title_fullStr Ophthalmic manifestations in Rothmund–Thomson syndrome: Case report and review of literature
title_full_unstemmed Ophthalmic manifestations in Rothmund–Thomson syndrome: Case report and review of literature
title_short Ophthalmic manifestations in Rothmund–Thomson syndrome: Case report and review of literature
title_sort ophthalmic manifestations in rothmund–thomson syndrome: case report and review of literature
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678305/
https://www.ncbi.nlm.nih.gov/pubmed/29044077
http://dx.doi.org/10.4103/ijo.IJO_89_17
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