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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Main Authors: Sherif Ali Eltawansy, Andrea Bakos, John Checton
Format: Article
Language:English
Published: Wiley 2015-01-01
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.
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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