The most common and important thrombophilic states are: the factor V Leiden mutation, the prothrombin gene G20210A mutation, antithrombin III deficiency, protein C and protein S deficiency [28] and the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism [29]. This evidence concerns the gene SERPINC1 and hyperinsulinemic hypoglycemia, familial, 4.