Cardiomyopathy
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Cardiomyopathies are diseases of the myocardium with associated structural and functional abnormalities. They represent a different group of disorders in which myocardium is itself structurally and functionally abnormal.
Load moreCardiomyopathies are diseases of the myocardium with associated structural and functional abnormalities. They represent a different group of disorders in which myocardium is itself structurally and functionally abnormal.
Cardiomyopathies are classified traditionally according to morphological and functional criteria into four categories: dilated cardiomyopathy (DCM), hypertrophic cardiomyopathy (HCM), restrictive cardiomyopathy (RCM) and arrhythmogenic right ventricular (RV) cardiomyopathy/dysplasia (ARVC/D).
DCM is the most common form of heart muscle disease, comprising approximately 60% of all cardiomyopathies and characterised by left ventricular (LV) dilation and systolic dysfunction. DCM is often assumed to be a common pathway of several cardiovascular pathologies.
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Videos
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Katelyn Storey, Scott W SharkeyUS Cardiology Review 2019;13(2):ePub: 26 August 2019.DOI: https://doi.org/10.15420/usc.2019.10.1
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Roland Tilz, Charlotte Eitel, Evgeny Lyan, et alArrhythmia & Electrophysiology Review 2019;8(3):173–9.DOI: https://doi.org/10.15420/aer.2019.31.3
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Douglas Ewan Cannie, Mohammed Majid Akhtar, Perry Elliott, et alEuropean Cardiology Review 2019;14(2):89–96DOI: https://doi.org/10.15420/ecr.2019.19.2
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Felipe Martinez, Eduardo Perna, Sergio V Perrone, et alEuropean Cardiology Review 2019;14(2):82–8DOI: https://doi.org/10.15420/ecr.2018.30.2
