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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2020
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| Materias: | |
| 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 |