Noncompaction Cardiomyopathy with Charcot-Marie-Tooth Disease
We report a case of a 53-year-old female presenting with a new-onset heart failure that was contributed secondary to noncompaction cardiomyopathy. The diagnosis was made by echocardiogram and confirmed by cardiac MRI. Noncompaction cardiomyopathy (also known as ventricular hypertrabeculation) is a n...
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Language: | English |
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Wiley
2015-01-01
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Series: | Case Reports in Cardiology |
Online Access: | http://dx.doi.org/10.1155/2015/646890 |
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author | Sherif Ali Eltawansy Andrea Bakos John Checton |
author_facet | Sherif Ali Eltawansy Andrea Bakos John Checton |
author_sort | Sherif Ali Eltawansy |
collection | DOAJ |
description | We report a case of a 53-year-old female presenting with a new-onset heart failure that was contributed secondary to noncompaction cardiomyopathy. The diagnosis was made by echocardiogram and confirmed by cardiac MRI. Noncompaction cardiomyopathy (also known as ventricular hypertrabeculation) is a newly discovered disease. It is considered to be congenital (genetic) cardiomyopathy. It is usually associated with genetic disorders and that could explain the genetic pathogenesis of the non-compaction cardiomyopathy. Our case had a history of Charcot-Marie-Tooth disease. There is a high incidence of arrhythmia and embolic complications. The treatment usually consists of the medical management, defibrillator placement, and lifelong anticoagulation. Heart transplantation will be the last resort. |
format | Article |
id | doaj-art-38a7fa07d1ec42c796659f84a87eb05b |
institution | Kabale University |
issn | 2090-6404 2090-6412 |
language | English |
publishDate | 2015-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Cardiology |
spelling | doaj-art-38a7fa07d1ec42c796659f84a87eb05b2025-02-03T01:22:55ZengWileyCase Reports in Cardiology2090-64042090-64122015-01-01201510.1155/2015/646890646890Noncompaction Cardiomyopathy with Charcot-Marie-Tooth DiseaseSherif Ali Eltawansy0Andrea Bakos1John Checton2Internal Medicine Department, Monmouth Medical Center, Long Branch, NJ 07740, USADrexel University College of Medicine, Philadelphia, PA 19129, USAInternal Medicine Department, Monmouth Medical Center, Long Branch, NJ 07740, USAWe report a case of a 53-year-old female presenting with a new-onset heart failure that was contributed secondary to noncompaction cardiomyopathy. The diagnosis was made by echocardiogram and confirmed by cardiac MRI. Noncompaction cardiomyopathy (also known as ventricular hypertrabeculation) is a newly discovered disease. It is considered to be congenital (genetic) cardiomyopathy. It is usually associated with genetic disorders and that could explain the genetic pathogenesis of the non-compaction cardiomyopathy. Our case had a history of Charcot-Marie-Tooth disease. There is a high incidence of arrhythmia and embolic complications. The treatment usually consists of the medical management, defibrillator placement, and lifelong anticoagulation. Heart transplantation will be the last resort.http://dx.doi.org/10.1155/2015/646890 |
spellingShingle | Sherif Ali Eltawansy Andrea Bakos John Checton Noncompaction Cardiomyopathy with Charcot-Marie-Tooth Disease Case Reports in Cardiology |
title | Noncompaction Cardiomyopathy with Charcot-Marie-Tooth Disease |
title_full | Noncompaction Cardiomyopathy with Charcot-Marie-Tooth Disease |
title_fullStr | Noncompaction Cardiomyopathy with Charcot-Marie-Tooth Disease |
title_full_unstemmed | Noncompaction Cardiomyopathy with Charcot-Marie-Tooth Disease |
title_short | Noncompaction Cardiomyopathy with Charcot-Marie-Tooth Disease |
title_sort | noncompaction cardiomyopathy with charcot marie tooth disease |
url | http://dx.doi.org/10.1155/2015/646890 |
work_keys_str_mv | AT sherifalieltawansy noncompactioncardiomyopathywithcharcotmarietoothdisease AT andreabakos noncompactioncardiomyopathywithcharcotmarietoothdisease AT johnchecton noncompactioncardiomyopathywithcharcotmarietoothdisease |