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Endothelial Nitric Oxide Synthase T-786C Mutation, Prothrombin Gene Mutation (G-20210-A) and Protein S Deficiency Could Lead to Myocardial Infarction in a Very Young Male Adult

INTRODUCTION: Myocardial infarction is a rare medical event in young people. The main reasons include congenital coronary abnormalities, coronary artery spasm, and coronary thrombosis due to hypercoagulable states (hereditary and acquired). AIM: We present a case of a young male adult with myocardia...

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Detalles Bibliográficos
Autores principales:	Klincheva, Milka, Vilarova, Elena Ambarkova, Angjusheva, Tanja, Milev, Ivan, Idoski, Enver, Mitrev, Zan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Institute of Immunobiology and Human Genetics 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884236/ https://www.ncbi.nlm.nih.gov/pubmed/27275349 http://dx.doi.org/10.3889/oamjms.2016.014

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