RESEARCH ARTICLE


An Overview of Cardiac Management in Neuromuscular Disease



Renee M. Hickey, John D. Cullen, George M. Sachs*
Department of Neurology, Brown University, Providence, Rhode Island, 02912, USA


Article Metrics

CrossRef Citations:
1
Total Statistics:

Full-Text HTML Views: 1716
Abstract HTML Views: 669
PDF Downloads: 305
ePub Downloads: 306
Total Views/Downloads: 2996
Unique Statistics:

Full-Text HTML Views: 932
Abstract HTML Views: 386
PDF Downloads: 215
ePub Downloads: 226
Total Views/Downloads: 1759



Creative Commons License
© Hickey et al.; Licensee Bentham Open.

open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.

* Address correspondence to this author at the Department of Neurology, Brown University, Providence, Rhode Island, 02912, USA; Tel: (401) 444-8761; Fax: (401) 444-3205; Email: gsachs@lifespan.org


Abstract

Muscular dystrophy and myasthenia gravis are two neuromuscular disorders that can involve significant cardiovascular complications. The frequency and severity of cardiac pathology varies widely among the muscular dystrophies. In some, it is nearly inevitable and requires regular evaluation. In others, assessment of cardiac function can be more symptom-driven. On-ly a minority of myasthenic patients manifest disease-related cardiovascular complications; however, their presentation can be rapidly progressive and life-threatening..

Keywords: Arrythmia, cardiomyopathy, muscular dystrophy, myasthenia gravis, myotonic dystrophy, treatment.