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Atypical presentation of Coats' Syndrome in facioscapulohumeral dystrophy - Reflecting the variation in phenotypic manifestations

PURPOSE: To report a unique case of atypical Coats' Syndrome in an 80 year old female with facioscapulohumeral dystrophy. OBSERVATIONS: An 80 years old female was diagnosed clinically of retinal telangiectasia with exudation threatening the fovia. She received a successful macular laser photoco...

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Autores principales: Akshikar, Rashmi, Feng, Rui, Gill, Kiranpreet, Chehade, Luke, Hughes, Edward
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061899/
https://www.ncbi.nlm.nih.gov/pubmed/30057966
http://dx.doi.org/10.1016/j.ajoc.2018.04.009
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author Akshikar, Rashmi
Feng, Rui
Gill, Kiranpreet
Chehade, Luke
Hughes, Edward
author_facet Akshikar, Rashmi
Feng, Rui
Gill, Kiranpreet
Chehade, Luke
Hughes, Edward
author_sort Akshikar, Rashmi
collection PubMed
description PURPOSE: To report a unique case of atypical Coats' Syndrome in an 80 year old female with facioscapulohumeral dystrophy. OBSERVATIONS: An 80 years old female was diagnosed clinically of retinal telangiectasia with exudation threatening the fovia. She received a successful macular laser photocoagulation with subsequent cessation of leakage. CONCLUSIONS AND IMPORTANCE: This case is in keeping with Coats' syndrome in fascioscapulohumeral dystrophy, which classically affects young male subjects - making this patient an obvious outlier. This once again reflects the variation in phenotypic manifestations of inherited disorders.
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spelling pubmed-60618992018-07-27 Atypical presentation of Coats' Syndrome in facioscapulohumeral dystrophy - Reflecting the variation in phenotypic manifestations Akshikar, Rashmi Feng, Rui Gill, Kiranpreet Chehade, Luke Hughes, Edward Am J Ophthalmol Case Rep Case report PURPOSE: To report a unique case of atypical Coats' Syndrome in an 80 year old female with facioscapulohumeral dystrophy. OBSERVATIONS: An 80 years old female was diagnosed clinically of retinal telangiectasia with exudation threatening the fovia. She received a successful macular laser photocoagulation with subsequent cessation of leakage. CONCLUSIONS AND IMPORTANCE: This case is in keeping with Coats' syndrome in fascioscapulohumeral dystrophy, which classically affects young male subjects - making this patient an obvious outlier. This once again reflects the variation in phenotypic manifestations of inherited disorders. Elsevier 2018-04-21 /pmc/articles/PMC6061899/ /pubmed/30057966 http://dx.doi.org/10.1016/j.ajoc.2018.04.009 Text en © 2018 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case report
Akshikar, Rashmi
Feng, Rui
Gill, Kiranpreet
Chehade, Luke
Hughes, Edward
Atypical presentation of Coats' Syndrome in facioscapulohumeral dystrophy - Reflecting the variation in phenotypic manifestations
title Atypical presentation of Coats' Syndrome in facioscapulohumeral dystrophy - Reflecting the variation in phenotypic manifestations
title_full Atypical presentation of Coats' Syndrome in facioscapulohumeral dystrophy - Reflecting the variation in phenotypic manifestations
title_fullStr Atypical presentation of Coats' Syndrome in facioscapulohumeral dystrophy - Reflecting the variation in phenotypic manifestations
title_full_unstemmed Atypical presentation of Coats' Syndrome in facioscapulohumeral dystrophy - Reflecting the variation in phenotypic manifestations
title_short Atypical presentation of Coats' Syndrome in facioscapulohumeral dystrophy - Reflecting the variation in phenotypic manifestations
title_sort atypical presentation of coats' syndrome in facioscapulohumeral dystrophy - reflecting the variation in phenotypic manifestations
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061899/
https://www.ncbi.nlm.nih.gov/pubmed/30057966
http://dx.doi.org/10.1016/j.ajoc.2018.04.009
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