%0 Case Reports
%T Hypertrophic cardiomyopathy in the systemic right ventricle in a patient with congenitally corrected transposition of the great arteries: A case report.
%A García-Cruz E
%A Manzur-Sandoval D
%A Toledo-Alemán EL
%A Angulo-Cruzado ST
%A Sánchez-López SV
%A Benita-Bordes A
%A Calderón-Colmenero J
%A Díaz-Gallardo LG
%A Aranda-Fraustro A
%A Mata-Salgado GD
%A Baranda-Tovar FM
%J Echocardiography
%V 40
%N 9
%D 2023 09 27
%M 37498200
%F 1.874
%R 10.1111/echo.15660
%X Congenitally corrected transposition of the great arteries is a rare clinical entity, which usually presents during adulthood with associated defects; atrioventricular block, heart failure, systemic valve failure, and arrhythmias usually complicate the clinical course. Even rarer is associated hypertrophic cardiomyopathy, which complicates the disease course and clinical decision-making. Herein, we present a patient with this condition who underwent heart transplantation, with adequate clinical resolution.