Association between haemophilia and inherited thrombophilia: A single centre survey

Haemophilia

Volumn 17, Issue 1, 2011, Pages 161-162

  Di Perna, C ^a   Franchini, M ^a   Riccardi, F ^a   Rivolta, G F ^a   Angeri, F ^a   Tagliaferri, A ^a  

^a UNIVERSITY HOSPITAL OF PARMA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5 LEIDEN; BLOOD CLOTTING FACTOR CONCENTRATE; PROTHROMBIN;

ADOLESCENT; ADULT; AGED; CHILD; DISEASE ASSOCIATION; DISEASE SEVERITY; FOLLOW UP; GENE MUTATION; GENETIC HETEROGENEITY; HEMARTHROSIS; HEMOPHILIA; HEMOPHILIA A; HUMAN; LETTER; MAJOR CLINICAL STUDY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEIN C DEFICIENCY; SCHOOL CHILD; THROMBOPHILIA;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; CHILD, PRESCHOOL; FACTOR V; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEMOPHILIA A; HEMOPHILIA B; HUMANS; INFANT; MALE; MIDDLE AGED; PHENOTYPE; SEVERITY OF ILLNESS INDEX; YOUNG ADULT;

EID: 79951868045     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2010.02358.x     Document Type: Letter

References (6)

1. Franchini M, Montagnana M, Targher G et al. Interpatient phenotypic inconsistency in severe congenital hemophilia: a systematic review of the role of inherited thrombophilia. Semin Thromb Haemost 2009; 35: 307-12.
2. Tagliaferri A, Di Perna C, Franchini M, Rivolta GF, Pattacini C. Hemophilia severity score system: validation from an Italian Regional Hemophilia Reference Center. J Thromb Haemost 2009; 7: 720-2.
3. Lee DH, Walker IR, Teitel J et al. Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A. Thromb Haemost 2000; 83: 387-91.
4. Escuriola-Ettingshausen C, Halimeh S, Kurnik K et al. Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors. Thromb Haemost 2001; 85: 218-20.
5. Arruda VR, Annichilo-Bizzacchi JM, Antunes SV, Costa FF. Association of severe hemophilia A and factor V Leiden: report of three cases. Haemophilia 1996; 2: 51-3.
6. Kurnik K, Kreuz W, Horneff S et al. Effects of the factor V G1691A mutation and the factor II G20210A variant on the clinical expression of severe hemophilia A in children - results of a multicenter studys. Haematologica 2007; 92: 982-5.