Case Report: ALCAPA syndrome: successful repair with an anatomical and physiological alternative surgical technique

Anomalous left coronary artery from the pulmonary artery, or ALCAPA syndrome, is a rare congenital cardiac disease that can cause myocardial infarction, heart failure and even death in paediatric patients. Only few untreated patients survive until adult age. Here we present the case of a 33-year-old...

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Detalles Bibliográficos
Autores principales: Vilá Mollinedo, Luis Gustavo, Jaime Uribe, Andrés, Aceves Chimal, José Luis, Martínez-Rubio, Roberto Pablo, Hernández-Romero, Karen Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4975369/
https://www.ncbi.nlm.nih.gov/pubmed/27547381
http://dx.doi.org/10.12688/f1000research.8823.2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4975369/
https://www.ncbi.nlm.nih.gov/pubmed/27547381
http://dx.doi.org/10.12688/f1000research.8823.2

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