“…Nutritional deficiencies B12, folate, protein C and S deficiency due to vitamin K deficiency [64,66] Genetic diseases MTHFR variants [39] Thrombophylic autoantibodies Antiphospholipid, antiprothrombin, antiphosfatidylserine/ prothrombin [17,22,26,27,45,47,52,53,55,66] Amino acid abnormalities Hyperhomocystinemia [41,48,[60][61][62][63]66] Autoimmune homology Mimicry between tTG/ factor XIII [67] Atherosclerosis Endothelial dysfunction [22,24] …”