Noonan syndrome associated with anomalous left coronary artery from the pulmonary artery in a patient with the rare RAF1 mutation: A case report and review of literature

We present the case of a 7-week-old male infant diagnosed with anomalous left coronary artery from the pulmonary artery (ALCAPA) who underwent repair by left coronary artery reimplantation, followed by an eventful postoperative period including need for venous arterial extracorporeal membrane oxygen...

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Detalles Bibliográficos
Autores principales: Garcia, Richard U, Safa, Raya, Evans, Chelsea, Alessio, Dominic, Delius, Ralph, Shehata, Bahig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716325/
https://www.ncbi.nlm.nih.gov/pubmed/31516287
http://dx.doi.org/10.4103/apc.APC_144_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716325/
https://www.ncbi.nlm.nih.gov/pubmed/31516287
http://dx.doi.org/10.4103/apc.APC_144_18

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