2016•University journal of medicine and medical specialitiesRequires access

Left ventricle involvement in Arrhythmogenic Right Ventricular Dysplasia

Manu Rajendran

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Abstract

Arrhythmogenic right ventricle dysplasia ARVD is an unusual progressive cardiomyopathy characterized by genetically determined fibrofatty replacement of myocardium, predominantly right ventricle with LBBB pattern ventricular arrhythmias. We have encountered a case of arrhythmogenic right ventricular dysplasia with RBBB type of ventricular tachycardia. We report this case because of rare association of RBBB pattern ventricular tachycardia in ARVD

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Arrhythmogenic right ventricle dysplasia ARVD is an unusual progressive cardiomyopathy characterized by genetically determined fibrofatty replacement of myocardium, predominantly right ventricle with LBBB pattern ventricular arrhythmias. We have encountered a case of arrhythmogenic right ventricular dysplasia with RBBB type of ventricular tachycardia. We report this case because of rare association of RBBB pattern ventricular tachycardia in ARVD

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Available abstract

Arrhythmogenic right ventricle dysplasia ARVD is an unusual progressive cardiomyopathy characterized by genetically determined fibrofatty replacement of myocardium, predominantly right ventricle with LBBB pattern ventricular arrhythmias. We have encountered a case of arrhythmogenic right ventricular dysplasia with RBBB type of ventricular tachycardia. We report this case because of rare association of RBBB pattern ventricular tachycardia in ARVD

Key concepts: Arrhythmogenic right ventricular dysplasia, Medicine, Ventricle, Cardiology, Internal medicine, Ventricular tachycardia, Dysplasia, Cardiomyopathy

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