Arrhythmogenic malignancies in hypertrophic cardiomyopathy

Shaji C. Menon; J. Martijn Bos; Steve R. Ommen; Michael J. Ackerman

doi:10.1007/978-1-84628-854-8_43

Arrhythmogenic malignancies in hypertrophic cardiomyopathy

Shaji C. Menon, J. Martijn Bos, Steve R. Ommen, Michael J. Ackerman

Cardiovascular Medicine

Research output: Chapter in Book/Report/Conference proceeding › Chapter

3 Scopus citations

Abstract

Cardiomyopathies are diseases of the myocardium associated with cardiac dysfunction. According to the World Health Organization (WHO) classification, cardiomyopathies are classified either as primary or secondary cardiomyopathies. Based on morphological and functional criteria, heritable cardiomyopathies are classified into four primary categories including hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), arrhythmogenic right ventricular cardiomyopathy (ARVC), and restrictive cardiomyopathy (RCM). More recently, left ventricular noncompaction (LVNC) syndrome has been added. Secondary cardiomyopathies include, for example, ischemic and hypertensive cardiomyopathy. This chapter focuses solely on HCM, with particular attention to its arrhythmogenic features.

Original language	English (US)
Title of host publication	Electrical Diseases of the Heart
Subtitle of host publication	Genetics, Mechanisms, Treatment, Prevention
Publisher	Springer London
Pages	610-626
Number of pages	17
ISBN (Print)	9781846288531
DOIs	https://doi.org/10.1007/978-1-84628-854-8_43
State	Published - Dec 1 2008

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Medicine(all)

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abstract = "Cardiomyopathies are diseases of the myocardium associated with cardiac dysfunction. According to the World Health Organization (WHO) classification, cardiomyopathies are classified either as primary or secondary cardiomyopathies. Based on morphological and functional criteria, heritable cardiomyopathies are classified into four primary categories including hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), arrhythmogenic right ventricular cardiomyopathy (ARVC), and restrictive cardiomyopathy (RCM). More recently, left ventricular noncompaction (LVNC) syndrome has been added. Secondary cardiomyopathies include, for example, ischemic and hypertensive cardiomyopathy. This chapter focuses solely on HCM, with particular attention to its arrhythmogenic features.",

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AU - Ommen, Steve R.

AU - Ackerman, Michael J.

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AB - Cardiomyopathies are diseases of the myocardium associated with cardiac dysfunction. According to the World Health Organization (WHO) classification, cardiomyopathies are classified either as primary or secondary cardiomyopathies. Based on morphological and functional criteria, heritable cardiomyopathies are classified into four primary categories including hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), arrhythmogenic right ventricular cardiomyopathy (ARVC), and restrictive cardiomyopathy (RCM). More recently, left ventricular noncompaction (LVNC) syndrome has been added. Secondary cardiomyopathies include, for example, ischemic and hypertensive cardiomyopathy. This chapter focuses solely on HCM, with particular attention to its arrhythmogenic features.

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Arrhythmogenic malignancies in hypertrophic cardiomyopathy

Abstract

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