Surgical treatment for anomalous origin of the right coronary artery from the pulmonary artery: a case report with five-year follow-up

BACKGROUND: Anomalous origin of the right coronary artery from the pulmonary artery (ARCAPA) is a rare congenital heart disease affecting about 0.002% of the population. Knowledge of ARCAPA is almost collected from case reports. The aim of this study was to provide a rare case to better understand t...

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Detalles Bibliográficos
Autores principales: Teng, Peng, Li, Weidong, Ni, Yiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789775/
https://www.ncbi.nlm.nih.gov/pubmed/33407633
http://dx.doi.org/10.1186/s13019-020-01374-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789775/
https://www.ncbi.nlm.nih.gov/pubmed/33407633
http://dx.doi.org/10.1186/s13019-020-01374-x

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