Budd-Chiari Syndrome in a Patient Heterozygous for the G20210A Mutation of the Prothrombin Gene

• References

• 1 Shill M, Henderson JM, Tavill AS. The Budd-Chiari syndrome revisited. The Gastroenterologist 1994; 2: 27-37.
• 2 Sugano S, Suzuki T, Makino H, Yanagimoto S, Nishio M, Onmura H, Iinuma M, Matuda T, Shinozawa Y. Budd-Chiari syndrome attributed to protein C deficiency. Am J Gastroenterol 1996; 91: 777-9.
• 3 Mahmoud AE, Wilde JT, Elias E. Budd-Chiari syndrome and factor V Leiden mutation. Lancet 1995; 345: 526.
• 4 Pelletier S, Landi B, Piette J-C, Ekert P, Coutellier A, Desmoulins C, Fadlallah JP, Herson S, Valla D. Antiphospholipid syndrome as the second cause of non-tumorous Budd-Chiari syndrome. J Hepatol 1994; 21: 76-80.
• 5 Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3’-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-703.
• 6 Phillips MD. Interrelated risk factors for venous thromboembolism. Circulation 1998; 95: 1749-51.