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Article

Hereditary thrombophilia as a cause of Budd-Chiari syndrome: A study from Western India

1 Oct 2001

Abstract excerpt

The inherited deficiencies of protein C, protein S, antithrombin III, factor V Leiden mutation, prothrombin gene polymorphism, and antiphospholipids were studied in 53 Budd-Chiari syndrome (BCS) and 33 portal vein thrombosis (PVT) cases and compared with 223 age- and sex-matched controls. Protein C deficiency was detected in 7 (13.2%), protein S in 3 (5.7%), and antithrombin III in 2 (3.8%) of the BCS cases....

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Identifiers

PMID: 11584361
DOI: 10.1053/jhep.2001.27948

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