Abstract：
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.
摘要：
先天性矫正的大动脉转位是一种罕见的临床实体，通常在成年期出现相关缺陷；房室传导阻滞，心力衰竭,系统阀门故障,心律失常通常会使临床过程复杂化。更罕见的是肥厚型心肌病，使病程和临床决策复杂化。在这里，我们介绍了一名患有这种疾病的患者，他接受了心脏移植，具有足够的临床分辨率。
