Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is an inherited myogenic disorder due to mutations in the dystrophin gene on chromosome Xp21.1. The clinical picture included peripheral muscle weakness, cardiomyopathy and chronic respiratory insufficiency. In this paper, the authors review cardiac involvement in p...

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Detalles Bibliográficos
Autores principales: Fayssoil, Abdallah, Abasse, Soumeth, Silverston, Katy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345647/
https://www.ncbi.nlm.nih.gov/pubmed/28269790
http://dx.doi.org/10.3233/JND-160194
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author Fayssoil, Abdallah
Abasse, Soumeth
Silverston, Katy
author_facet Fayssoil, Abdallah
Abasse, Soumeth
Silverston, Katy
author_sort Fayssoil, Abdallah
collection PubMed
description Duchenne muscular dystrophy (DMD) is an inherited myogenic disorder due to mutations in the dystrophin gene on chromosome Xp21.1. The clinical picture included peripheral muscle weakness, cardiomyopathy and chronic respiratory insufficiency. In this paper, the authors review cardiac involvement in patients with DMD, propose a cardiac impairment classification and discuss therapeutic management options.
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spelling pubmed-53456472017-03-24 Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy Fayssoil, Abdallah Abasse, Soumeth Silverston, Katy J Neuromuscul Dis Review Duchenne muscular dystrophy (DMD) is an inherited myogenic disorder due to mutations in the dystrophin gene on chromosome Xp21.1. The clinical picture included peripheral muscle weakness, cardiomyopathy and chronic respiratory insufficiency. In this paper, the authors review cardiac involvement in patients with DMD, propose a cardiac impairment classification and discuss therapeutic management options. IOS Press 2017-02-28 /pmc/articles/PMC5345647/ /pubmed/28269790 http://dx.doi.org/10.3233/JND-160194 Text en IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Fayssoil, Abdallah
Abasse, Soumeth
Silverston, Katy
Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy
title Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy
title_full Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy
title_fullStr Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy
title_full_unstemmed Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy
title_short Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy
title_sort cardiac involvement classification and therapeutic management in patients with duchenne muscular dystrophy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345647/
https://www.ncbi.nlm.nih.gov/pubmed/28269790
http://dx.doi.org/10.3233/JND-160194
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