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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Detalhes bibliográficos
Publicado no:F1000Res
Main Authors: Vilá Mollinedo, Luis Gustavo, Jaime Uribe, Andrés, Aceves Chimal, José Luis, Martínez-Rubio, Roberto Pablo, Hernández-Romero, Karen Patricia
Formato: Artigo
Idioma:Inglês
Publicado em: F1000Research 2016
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Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4975369/
https://ncbi.nlm.nih.gov/pubmed/27547381
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.8823.2
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