Recurrent coronary syndromes in a patient with isolated very-high lipoprotein (a) and the prothrombin genetic variant rs1799963 (G20210A): a case report

BACKGROUND: Elevated lipoprotein (a) [Lp(a)] is an under-diagnosed genetically inherited risk factor for coronary heart disease (CHD) and calcific aortic valve stenosis. Premature myocardial infarction (MI) could stem from the association between elevated Lp(a) and other non-traditional cardiovascul...

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Detalles Bibliográficos
Autores principales: Khantalin, Ilya, Blanchard, Valentin, Viallet, Nicolas, Lambert, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439380/
https://www.ncbi.nlm.nih.gov/pubmed/31020261
http://dx.doi.org/10.1093/ehjcr/ytz019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439380/
https://www.ncbi.nlm.nih.gov/pubmed/31020261
http://dx.doi.org/10.1093/ehjcr/ytz019

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