Article

Inherited Prothrombotic Defects in Budd-Chiari Syndrome and Portal Vein Thrombosis

2004-06-01

Abstract excerpt

We studied 57 patients with Budd-Chiari syndrome (BCS) and 48 with portal vein thrombosis (PVT) for underlying inherited prothrombotic defects such as protein C, protein S, and antithrombin III deficiencies. Genetic mutations for factor V Leiden, prothrombin gene 20210A, and methyltetrahydrofolate reductase (MTHFR) C677T were studied in 29 patients in each group. Inherited prothrombotic defects were detected in 16...

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Literature Corpus work: 80eaab4b-571d-566c-bc9d-539440db0475
DOI: 10.1309/f2u1xbv4rxyuayg0

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