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Article

[Multigenic thrombophilia: genetic anomaly of factor II and mutation of factor V Leiden. Study in a French family].

Presse medicale (Paris, France : 1983) - 14 Jun 1997

Conard J, Mabileau-Brouzes C, Horellou M H, Elalamy I, Samama M M

Abstract excerpt

BACKGROUND: A genetic variation of the prothrombin (factor II) gene, a G to A transition at nucleotide position 20210, was recently found in patients with familial thrombophilia (predisposition to venous thrombosis). It seems to be frequent in patients with the factor V Leiden mutation. We report a family with the factor V Leiden and/or the genetic variation of prothrombin in 3 members. CASE REPORT: The patient...

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PMID: 9238178

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

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Related research

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[Multigenic thrombophilia: genetic anomaly of factor II and mutation of factor V Leiden. Study in a French family].PMID 9238178Read ↗

[Heterozygous prothrombin gene mutation G20210A and associated diseases].Semantic proximity Read ↗

Clinical and Molecular Study of Common Thrombophilia Mutation Prothrombin G20210A.Semantic proximity Read ↗

[20210A mutation of the prothrombin and venous thromboembolism gene].Semantic proximity Read ↗

Clinical and analytical relevance of the combination of prothrombin 20210A/A and factor V Leiden: results from a large family.Semantic proximity Read ↗

Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.Semantic proximity Read ↗

[20210G/A mutation of prothrombin gene in a patient with deep venous thrombosis ad pulmonary embolism without other risk factors of thrombosis].Semantic proximity Read ↗

[Prevalence of Factor V Leiden and the G20210A mutation of the prothrombin gene in a random group of patients with thrombotic episodes].Semantic proximity Read ↗

Coinheritance of factor V Leiden (F5 1691A) and prothrombin 20210 A (F2 20210A) in an Austrian family as cause for early onset of venous thromboembolism.Semantic proximity Read ↗

Coexistence of three genetic risk factors in a Spanish thrombophilic family: Factor V Leiden, prothrombin 20210 and a new type I antithrombin deficiency.Semantic proximity Read ↗

[Coincidence of 20210A prothrombin variant and factor V Leiden predisposing to venous thromboembolism].Semantic proximity Read ↗

[G20210A transition in the prothrombin gene and venous thromboembolic disease].Semantic proximity Read ↗

Prothrombin G20210A gene mutation, heparin cofactor II defects, primary (essential) thrombocythemia, and thrombohemorrhagic manifestations.Semantic proximity Read ↗

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