We report a case ofmyocardial infarction at a young age in a subject heterozygous for the G20210A prothrombin gene variant and homozygous for the C677TMTHFR polymorphism, who presented a strong family history of atherothrombosis. Genetic screening for inherited thrombophilia, especially in the presence of a strong familiarity, may be a critical information for secondary prevention of arterial thrombosis.

A case report of myocardial infarction in young patient with a parental history of premature cardiovascular death: Combination of prothrombotic gene mutations

Botto N;Mariani M;
2008

Abstract

We report a case ofmyocardial infarction at a young age in a subject heterozygous for the G20210A prothrombin gene variant and homozygous for the C677TMTHFR polymorphism, who presented a strong family history of atherothrombosis. Genetic screening for inherited thrombophilia, especially in the presence of a strong familiarity, may be a critical information for secondary prevention of arterial thrombosis.
2008
Istituto di Fisiologia Clinica - IFC
Myocardial infarction
C677T methylenetetrahydrofolate reductase
Prothrombin G20210A mutation
Genetic testing
Thrombotic risk
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/46066
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