Arrhythmogenic right ventricular dysplasia/cardiomyopathy was first reported as the partial replacement of the right ventricular myocardium by fat or fibrous tissue. In 1965, researchers described the ...
A Case of Cardiac Sarcoidosis Concealed by Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
This arrhythmia commonly occurs in the absence of structural heart disease and is typically benign. This condition shares a similar pathogenesis to ARVD/C. Patients with the adult form demonstrate ...
The following is a summary of “Arrhythmogenic Right Ventricular Cardiomyopathy: the importance of biventricular strain in ...
Arrhythmogenic right ventricular dysplasia, or ARVD — also known as arrhythmogenic right ventricular cardiomyopathy, or ARVC — is a genetic condition (autosomal dominant) affecting the ...
Differential diagnosis with arrhythmogenic right ventricular cardiomyopathy (ARVC) constitutes a frequent problem, especially in athletes showing ventricular arrhythmias with left bundle branch block ...
Cardiac sarcoidosis and ACM genetic variants coexist with distinct features, highlighting the need for refined clinical ...
Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) has major implications for the management of patients and their first-degree relatives. Diagnosis is based on a set ...
The classic ECG findings in arrhythmogenic right ventricular dysplasia are inverted T waves in the right precordial leads (V1-V3) with an epsilon wave after the QRS in lead V1, representing early ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback