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Muscular Dystrophy and Heart Failure: An Unusual Association
Type one muscular dystrophy (DM1) is the most common inherited muscular dystrophy in the adult population. Typically, DM1 presents as myotonia, muscle weakness, cataracts, and cardiac abnormalities, mainly in the conduction system. Although left ventricular dysfunction is not the most common manifes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cureus
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577820/ https://www.ncbi.nlm.nih.gov/pubmed/34786221 http://dx.doi.org/10.7759/cureus.18604 |
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author | Pais, João P Sousa, Marta B Cambão, Ana R Nascimento, Ana Guerra, Diana |
author_facet | Pais, João P Sousa, Marta B Cambão, Ana R Nascimento, Ana Guerra, Diana |
author_sort | Pais, João P |
collection | PubMed |
description | Type one muscular dystrophy (DM1) is the most common inherited muscular dystrophy in the adult population. Typically, DM1 presents as myotonia, muscle weakness, cataracts, and cardiac abnormalities, mainly in the conduction system. Although left ventricular dysfunction is not the most common manifestation of DM1, it can be seen with disease progression. The presentation of DM1 as a de novo heart failure is unusual, making its diagnosis a clinical challenge. |
format | Online Article Text |
id | pubmed-8577820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-85778202021-11-15 Muscular Dystrophy and Heart Failure: An Unusual Association Pais, João P Sousa, Marta B Cambão, Ana R Nascimento, Ana Guerra, Diana Cureus Cardiology Type one muscular dystrophy (DM1) is the most common inherited muscular dystrophy in the adult population. Typically, DM1 presents as myotonia, muscle weakness, cataracts, and cardiac abnormalities, mainly in the conduction system. Although left ventricular dysfunction is not the most common manifestation of DM1, it can be seen with disease progression. The presentation of DM1 as a de novo heart failure is unusual, making its diagnosis a clinical challenge. Cureus 2021-10-08 /pmc/articles/PMC8577820/ /pubmed/34786221 http://dx.doi.org/10.7759/cureus.18604 Text en Copyright © 2021, Pais et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Cardiology Pais, João P Sousa, Marta B Cambão, Ana R Nascimento, Ana Guerra, Diana Muscular Dystrophy and Heart Failure: An Unusual Association |
title | Muscular Dystrophy and Heart Failure: An Unusual Association |
title_full | Muscular Dystrophy and Heart Failure: An Unusual Association |
title_fullStr | Muscular Dystrophy and Heart Failure: An Unusual Association |
title_full_unstemmed | Muscular Dystrophy and Heart Failure: An Unusual Association |
title_short | Muscular Dystrophy and Heart Failure: An Unusual Association |
title_sort | muscular dystrophy and heart failure: an unusual association |
topic | Cardiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577820/ https://www.ncbi.nlm.nih.gov/pubmed/34786221 http://dx.doi.org/10.7759/cureus.18604 |
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