Case report of asymptomatic very late presentation of ALCAPA syndrome: review of the literature since pathophysiology until treatment

BACKGROUND: Anomalous origin of the left coronary artery (LCA) from the pulmonary artery (ALCAPA) is an unusual congenital heart defect which affects approximately 1 in 300 000 live births and accounts for 0.5% of all congenital heart disease. Without surgical intervention, most patients die in infa...

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Detalles Bibliográficos
Autores principales: Cambronero-Cortinas, Esther, Moratalla-Haro, Pedro, González-García, Ana Elvira, Oliver-Ruiz, José María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780492/
https://www.ncbi.nlm.nih.gov/pubmed/33426460
http://dx.doi.org/10.1093/ehjcr/ytaa257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780492/
https://www.ncbi.nlm.nih.gov/pubmed/33426460
http://dx.doi.org/10.1093/ehjcr/ytaa257

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