ALCAPA syndrome, a rare cause of sudden cardiac death.
作者信息
Rehman Muniebur, Braber Thijs, Mouden Mohamed, Knollema Siert, Güçlü Ahmet
机构信息
Department of Cardiology, Isala Heart Centre, Zwolle, The Netherlands.
Department of Nuclear Medicine, Isala Heart Centre, Zwolle, The Netherlands.
出版信息
Neth Heart J. 2024 Apr;32(4):184-186. doi: 10.1007/s12471-023-01829-5. Epub 2023 Nov 28.
Abstract
摘要
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本文引用的文献
1
Case report of asymptomatic very late presentation of ALCAPA syndrome: review of the literature since pathophysiology until treatment.左冠状动脉起源于肺动脉综合征（ALCAPA综合征）无症状极晚期表现的病例报告：从病理生理学到治疗的文献综述
Eur Heart J Case Rep. 2020 Sep 19;4(5):1-5. doi: 10.1093/ehjcr/ytaa257. eCollection 2020 Oct.
2
2020 ESC Guidelines for the management of adult congenital heart disease.2020年欧洲心脏病学会成人先天性心脏病管理指南。
Eur Heart J. 2021 Feb 11;42(6):563-645. doi: 10.1093/eurheartj/ehaa554.
3
Case Report: ALCAPA syndrome: successful repair with an anatomical and physiological alternative surgical technique.病例报告：左冠状动脉起源于肺动脉综合征：采用解剖学和生理学替代手术技术成功修复
F1000Res. 2016 Jul 13;5:1680. doi: 10.12688/f1000research.8823.2. eCollection 2016.
4
Coronary artery anomalies overview: The normal and the abnormal.冠状动脉异常概述：正常与异常情况
World J Radiol. 2016 Jun 28;8(6):537-55. doi: 10.4329/wjr.v8.i6.537.
5
Anomalous origin of the left coronary artery from the pulmonary artery in adults: a comprehensive review of 151 adult cases and a new diagnosis in a 53-year-old woman.成人左冠状动脉起自肺动脉：151 例成人病例的综合回顾及 1 例 53 岁女性新诊断。
Clin Cardiol. 2011 Apr;34(4):204-10. doi: 10.1002/clc.20848.
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