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Arrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural …
2015年10月16日 · AR‐DCM indicates arrhythmogenic dilated cardiomyopathy; SCD/SVT/VF, sudden cardiac death, sustained ventricular tachycardia, and ventricular fibrillation.
Arrhythmogenic Cardiomyopathy | Circulation Research
2017年9月15日 · Arrhythmogenic cardiomyopathy (AC) is an inherited form of heart disease characterized pathologically by fibrofatty myocardial replacement and clinically by prominent ventricular arrhythmias and impairment of ventricular systolic function.
Arrhythmias in Dilated Cardiomyopathy: Diagnosis and Treatment
2019年5月18日 · Patients with dilated cardiomyopathy (DCM) can develop a broad range of bradyrhythmias and tachyarrhythmias including sinus node dysfunction, various degrees of atrioventricular block, interventricular conduction delay, and atrial and ventricular arrhythmias.
Arrhythmogenic Cardiomyopathy: Definition, Classification and ...
Arrhythmogenic cardiomyopathy (ACM) is an inherited heart muscle disease with a prevalence of approximately 1:5000 , characterized by fibro-fatty myocardial tissue replacement and correlated risk of ventricular arrhythmic events (VA) and sudden cardiac death (SCD), especially in …
Arrhythmogenic Cardiomyopathy | ACM & ARVC | Penn Medicine
What Is Arrhythmogenic Cardiomyopathy (ACM)? Arrhythmogenic cardiomyopathy (ACM) is a condition in the myocardium, the heart's muscular wall. A defect in proteins that connect heart muscle cells (myocytes) causes the cells to die. They are replaced by scar tissue and fatty cells.
Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: …
This review summarizes the current knowledge of hypertrophic, dilated and arrhythmogenic cardiomyopathy with a particular emphasis on their pathophysiology, clinical features, and diagnostic approach.
Dilated Cardiomyopathy Overview - GeneReviews® - NCBI Bookshelf
2007年7月27日 · Note: Arrhythmogenic right ventricular cardiomyopathy (ARVC) with predominant left ventricular involvement may present as DCM [Sen-Chowdhry et al 2008]. DCM usually initially manifests in adults in the fourth to sixth decade, although it may present at any age (prenatally; in infancy, early or late childhood, or adolescence; or in the elderly).
Arrhythmogenic Cardiomyopathy | Circulation - AHA/ASA Journals
2011年10月11日 · Arrhythmogenic cardiomyopathy is the most arrhythmogenic form of human heart disease and a major cause of sudden death in the young. 1,2 Originally described as a right ventricular disease (arrhythmogenic right ventricular cardiomyopathy), 3 it is now recognized to include a spectrum of biventricular and left-dominant forms that may be ...
2019 HRS Expert Consensus Statement on Evaluation, Risk …
2020年4月21日 · Arrhythmogenic cardiomyopathy is a broad diagnosis that includes any ventricular dysfunction not caused by ischemic, hypertensive, or valvular heart disease in which arrhythmia (including atrial fibrillation, ventricular arrhythmia, and conduction disease) is part of the clinical presentation. 1 This includes the relatively well-defined ...
Emerging concepts in arrhythmogenic dilated cardiomyopathy
Dilated cardiomyopathy (DCM) represents one of the primary cardiomyopathies and may lead to heart failure and sudden death. Until recently, ventricular arrhythmias were considered to be a direct consequence of the systolic dysfunction of the left ventricle (LV) and guidelines for implantable cardiov …