Distinguish Rare Dual Left Anterior Descending Artery with Anomalous Origins in Asymptomatic Patients  

作　　者：Wen Zhang Ting Wu Xijian Chen Hong Luo Yifei Li 

机构地区：[1]Key Laboratory of Birth Defects and Related Diseases of Women and Children of Ministry of Education(MOE),West China Second University Hospital,Sichuan University,Chengdu,610000,China [2]Department of Ultrasonic Medicine,West China Second University Hospital,Sichuan University,Chengdu,610000,China [3]Department of Radiology,West China Second University Hospital,Sichuan University,Chengdu,610000,China [4]Department of Pediatrics,West China Second University Hospital,Sichuan University,Chengdu,610000,China

出　　处：《Congenital Heart Disease》2024年第4期399-406,共8页先天性心脏病（英文）

基　　金：supported by grants from the National Natural Science Foundation of China (82270249).

摘　　要：To the Editor Congenital coronary artery anomalies(CAAs)are characterized by abnormalities in the origins,course,or termination of the three main epicardial coronary arteries[1,2].These anomalies can result in a spectrum of clinical manifestations,from chest pain and angina to more severe conditions such as microcirculation disorders,heart failure,or even sudden cardiac death.Among CAAs,the duplication of the left anterior descending artery(LAD)is particularly rare and usually misdiagnosed[3].

关 键 词：CORONARY ANGINA ARTERIES 

分 类 号：R541.4[医药卫生—心血管疾病]