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

Thromb Haemost 1998; 79(02): 445-446
DOI: 10.1055/s-0037-1615008

Scientific and Standardization Committee Communication

Schattauer GmbH

Paolo Bucciarelli

¹From the Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and University of Milan, Italy

,

Franca Franchi

¹From the Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and University of Milan, Italy

,

Adriano Alatri

¹From the Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and University of Milan, Italy

,

Paola Bettini

¹From the Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and University of Milan, Italy

,

Marco Moia

¹From the Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, IRCCS Maggiore Hospital and University of Milan, Italy

References
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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.
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