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Histopathological features and myocyte detachment in arrhythmogenic right ventricular cardiomyopathy/dysplasia. 26

Histopathological features and myocyte detachment in arrhythmogenic right ventricular cardiomyopathy/dysplasia. 26

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Figure 1: ECG shows PVCs in the pattern of bigemini, trigemini, and...
Figure 2: Cardiac MRI shows mild dilatation of the right atrium and the...
Figure 4: Histopathological features and myocyte detachment in...
Arrhythmogenic right ventricular cardiomyopathy or dysplasia: a case report
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  • Jul 2023
Arrhythmogenic cardiomyopathy (ACM) is a progressive genetic disease of the myocardium characterized by loss of myocardial cells and replacement by fibrofatty tissue in the right and/or left ventricle (RV/LV), clinically manifested by syncope, palpitations, heart failure, or sudden cardiac death (SCD). We presented a case where the patient suffered...
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Detection of gene mutation in the prognosis of a patient with arrhythmogenic right ventricular cardiomyopathy: a case report
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Background Arrhythmogenic right ventricular cardiomyopathy (ARVC), or more recently known as arrhythmogenic cardiomyopathy (ACM), is an heritable disorder of the myocardium characterized by progressive fibrofatty replacement the heart muscle and risk of ventricular arrhythmias and sudden cardiac death (SCD). We report a case study to demonstrate th...
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