Prothrombin gene G20210A mutation and elevated anticardiolipin antibodies in a patient with combined portal-mesenteric vein thrombosis

Intensive Care Medicine

Volumn 26, Issue 10, 2000, Pages 1571-1574

  Friederich, Patrick ^a   Putensen, Christian ^a   Stüber, Frank ^a  

^a UNIVERSITY HOSPITAL BONN   (Germany)

Author keywords

Chromosome 11; Coagulation; G20210A mutation; Genetic risk; Prothrombin; Thrombosis

Indexed keywords

ANTIVITAMIN K; CARDIOLIPIN ANTIBODY; HEPARIN; PROTHROMBIN;

ABDOMINAL DISTENSION; ADULT; ANTICOAGULANT THERAPY; ARTICLE; ARTIFICIAL VENTILATION; CASE REPORT; GENE MUTATION; HEPARINIZATION; HUMAN; LAPAROTOMY; MALE; MESENTERIC VEIN THROMBOSIS; PORTAL VEIN THROMBOSIS; RETROPERITONEAL HEMATOMA; THROMBECTOMY;

ADULT; ANTIBODIES, ANTICARDIOLIPIN; ANTICOAGULANTS; CASE REPORT; CAUSALITY; HEMATOMA; HEPARIN; HUMAN; IMMUNOGLOBULIN G; MALE; MESENTERIC VASCULAR OCCLUSION; MESENTERIC VEINS; MUTATION; PARTIAL THROMBOPLASTIN TIME; PORTAL VEIN; PROTHROMBIN; THROMBECTOMY; VENOUS THROMBOSIS;

EID: 0033792553     PISSN: 03424642     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001340000652     Document Type: Article

References (10)

1. Venous thrombosis: A multicausal disease
2. Frequent factor II G20210A mutation in idiopathic portal vein thrombosis
3. Antiphospholipid antibodies and thrombosis
4. Transient lupus anticoagulant associated with prothrombin deficiency: Unusual cause of bleeding in a 5-year-old girl
5. Extrahepatic portal venous thrombosis: Frequent recognition of associated diseases
6. Mesenteric venous thrombosis due to antithrombin III deficiency
7. Portal and mesenteric thrombosis revealing constitutional protein C deficiency
8. Mesenteric venous thrombosis: Still a lethal disease in the 1990s
9. Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene
10. Portal and mesenteric venous thrombosis in a patient heterozygous for the 20210 A allele of the prothrombin gene