ALCAPA syndrome, a rare cause of sudden cardiac death
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12471-023-01829-5.pdf
Reference5 articles.
1. Cambronero-Cortinas E, Moratalla-Haro P, González-García AE, et al. Case report of asymptomatic very late presentation of ALCAPA syndrome: review of the literature since pathophysiology until treatment. Eur Heart J Case Rep. 2020;4:1–5.
2. Yau JM, Singh R, Halpern EJ, et al. 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. Clin Cardiol. 2011;34:204–10.
3. Baumgartner H, De Backer J, Babu-Narayan SV, et al. ESC guidelines for the management of adult congenital heart disease. Eur Heart J. 2020;2020:563–645.
4. Villa ADM, Sammut E, Nair A, et al. Coronary artery anomalies overview: the normal and the abnormal. World J Radiol. 2016;8:537.
5. Vilá Mollinedo LG, Uribe JA, Aceves Chimal JL, et al. Case report: ALCAPA syndrome: successful repair with an anatomical and physiological alternative surgical technique. F1000Res. 2016;5:1680.
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