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Article

Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis: a study from North India.

American journal of clinical pathology - 1 Jun 2004

Bhattacharyya Maitreyee, Makharia Govind, Kannan M, Ahmed R P H, Gupta P K, Saxena Renu

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...

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PMID: 15198356
DOI: 10.1309/F2U1-XBV4-RXYU-AYG0

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MTHFR

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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