Angiographic diagnosis of ALCAPA syndrome in an adult
Abstract
The anomalous origin of the left coronary artery from the main pulmonary artery is a relatively common congenital heart disease. In spite of its high mortality in the first year of life, those patients affected by this condition may reach adulthood. The case of a 28-year-old woman with this disease, and its angiographic diagnosis, is reported.Downloads
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Published
2015-10-11
How to Cite
1.
Rodríguez Blanco S, Leyva Quert A, Valdés Recarey M, Mendoza Ortiz JL, Ponte González G, Aguilar Medina JM, et al. Angiographic diagnosis of ALCAPA syndrome in an adult. CorSalud [Internet]. 2015 Oct. 11 [cited 2025 Jun. 27];7(4):318-21. Available from: https://revcorsalud.sld.cu/index.php/cors/article/view/80
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CASE REPORTS
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