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A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis
Facioscapulohumeral muscular dystrophy (FSHD) is a common inherited muscular dystrophy presented clinically with slowly progressive weakness and wasting of facial and limb muscles and rare bulbar muscle involvement. We present herein a 70-year-old man who was a known case of FSHD with complaint of 1...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829232/ https://www.ncbi.nlm.nih.gov/pubmed/24250856 |
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author | Asadollahi, Marjan Rezaiyan, Bibiseyedeh Amjadi, Hiva |
author_facet | Asadollahi, Marjan Rezaiyan, Bibiseyedeh Amjadi, Hiva |
author_sort | Asadollahi, Marjan |
collection | PubMed |
description | Facioscapulohumeral muscular dystrophy (FSHD) is a common inherited muscular dystrophy presented clinically with slowly progressive weakness and wasting of facial and limb muscles and rare bulbar muscle involvement. We present herein a 70-year-old man who was a known case of FSHD with complaint of 15-day history of progressive difficulty in chewing and dysarthria and was found to have myasthenia gravis. Related literatures have been also reviewed. |
format | Online Article Text |
id | pubmed-3829232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-38292322013-11-18 A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis Asadollahi, Marjan Rezaiyan, Bibiseyedeh Amjadi, Hiva Iran J Neurol Case Report Facioscapulohumeral muscular dystrophy (FSHD) is a common inherited muscular dystrophy presented clinically with slowly progressive weakness and wasting of facial and limb muscles and rare bulbar muscle involvement. We present herein a 70-year-old man who was a known case of FSHD with complaint of 15-day history of progressive difficulty in chewing and dysarthria and was found to have myasthenia gravis. Related literatures have been also reviewed. Tehran University of Medical Sciences 2012 /pmc/articles/PMC3829232/ /pubmed/24250856 Text en Copyright © 2012 Iranian Neurological Association, and Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Case Report Asadollahi, Marjan Rezaiyan, Bibiseyedeh Amjadi, Hiva A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis |
title | A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis |
title_full | A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis |
title_fullStr | A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis |
title_full_unstemmed | A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis |
title_short | A rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis |
title_sort | rare case of facioscapulohumeral muscular dystrophy and myasthenia gravis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829232/ https://www.ncbi.nlm.nih.gov/pubmed/24250856 |
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