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Arrhythmogenic right ventricular cardiomyopathy complicating hypertrophic cardiomyopathy. 2022

Yoshihiko Kagawa, and Ryuji Okamoto, and Yoshihiro Asano, and Yasushi Sakata, and Kaoru Dohi
Department of Cardiology and Nephrology, Mie University Graduate School of Medicine, Tsu, Mie, Japan.

UI MeSH Term Description Entries
D002312 Cardiomyopathy, Hypertrophic A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY). Cardiomyopathy, Hypertrophic Obstructive,Cardiomyopathies, Hypertrophic,Cardiomyopathies, Hypertrophic Obstructive,Hypertrophic Cardiomyopathies,Hypertrophic Cardiomyopathy,Hypertrophic Obstructive Cardiomyopathies,Hypertrophic Obstructive Cardiomyopathy,Obstructive Cardiomyopathies, Hypertrophic,Obstructive Cardiomyopathy, Hypertrophic
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D019571 Arrhythmogenic Right Ventricular Dysplasia A congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the RIGHT VENTRICLE wall and loss of myocardial cells. Primary injuries usually are at the free wall of right ventricular and right atria resulting in ventricular and supraventricular arrhythmias. Arrhythmogenic Right Ventricular Cardiomyopathy,Right Ventricular Dysplasia, Arrhythmogenic,Ventricular Dysplasia, Right, Arrhythmogenic,ARVD-C,Arrhythmogenic Right Ventricular Cardiomyopathy-Dysplasia,Arrhythmogenic Right Ventricular Dysplasia-Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy Dysplasia

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