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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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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. |
format | Online Article Text |
id | pubmed-6061899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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