Combined factor V and factor VII deficiency due to an independent segregation of the two defects

Clinical and Applied Thrombosis/Hemostasis

Volumn 5, Issue 2, 1999, Pages 136-138

  Girolami, Antonio ^a,b   Zanon, Ezio ^a   Bertomoro, Antonella ^a   Gavasso, Sabrina ^a   Fadin, Mariangela ^a  

^a UNIVERSITY OF PADUA MEDICAL SCHOOL   (Italy)

^b Institute of Medical Semeiotics   (Italy)

Author keywords

Combined defect; Factor V deficiency; Factor VII deficiency

Indexed keywords

ADOLESCENT; ARTICLE; BLOOD CLOTTING FACTOR 5 DEFICIENCY; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CASE REPORT; CLINICAL FEATURE; COMORBIDITY; FAMILY STUDY; GENE SEGREGATION; HETEROZYGOTE; HUMAN; MALE; PARTIAL THROMBOPLASTIN TIME; PEDIGREE ANALYSIS; PRIORITY JOURNAL; PROTHROMBIN TIME;

EID: 0032891230     PISSN: 10760296     EISSN: None     Source Type: Journal    
DOI: 10.1177/107602969900500211     Document Type: Article

References (16)

1. Girolami A. Factor VII mangel unt varianten. Haemostareolosis 1984;3:98.
2. Girolami A, Brunetti A, De Marco L. Congenital combined factor V deficiency and factor VIII deficiency in a male born from a brother-sister incest. Blut 1974;28:33.
3. Girolami A, Dal Bo Zanon R, Fabris F, Franzoso R, Combined factor VII and factor VIII deficiency due to a casual association of heterozygosis for factor VII deficiency and haemophilia A. Acta Haematol 1977;58:246.
4. Girolami A, Dal Bo Zanon R, De Marco L, Cappellato G. Hemophilia B with associated factor VII deficiency. A distinct variant of hemophilia B with low factor VII activity and normal factor VII antigen. Blut 1980;40:267.
5. Soff GA, Levin J. Familial multiple coagulation factor deficiencies. Review of literature: differentiation of single hereditary disorders associated with multiple factor deficiencies from coincidental concurrence of single factor deficiency states. Semin Thromb Hemost 1981;7:112.
6. Girolami A, Sticchi A, Burul A, Dal Bo Zanon R. An immunological investigation of haemophilia B with a tentative classification of the disease into five variants. Vox Sang 1977;32:230.
7. Rotoli B, D'Avino R, Chiurazzi F. Combined Factor V and factor VII deficiency. Acta Haematol 1983;69:117.
8. Ambriz-Fernandez HR, Villasenor A, Reyna MP, et al. Coagulation factors V and VII combined congenital deficiency in a Mexican family: Toledo-Tehuantepec deficiency, a new pathological entity. Arch Invest Med (Mex) 1985;16:59.
9. Girolami A, Fabris F, Dal Bo Zanon R, Burul A. Factor VII Padua: a congenital coagulation disorder due to abnormal factor VII with a peculiar activation pattern. J Lab Clin Med 1978;91:387.
10. Girolami A, Simioni P, Venturelli U, et al. Factor V antigen levels in APC resistance, in factor V deficiency and in combined APC resistance and factor V deficiency (pseudohomozygosis for APC resistance). Blood Coagul Fibrinolysis 1997;8:245.
11. Ragni MV, Levis JH, Spero JA, Hasiba U. Factor VII deficiency. Br J Haematol 1981;10:79.
12. Triplett DA, Brandt JT, Batard MA, et al. Hereditary factor VII deficiency:heterogeneity defined by combined functional and immunochemical analysis. Blood 1985;66:1284.
13. Girolami A, Sartori MT, Zerbinati P. Frequent association of factor VII defect with other clotting disorders. Blood Coagul Fibrinolysis 1992;3:829.
14. Tracy PB, Mann KG. Abnormal formation of the prothrombinase complex factor V deficiency and related disorder. Hum Pathol 1987;18:162.
15. Girolami A, Simioni P, Scarano L, et al. Hemorrhagic and thrombotic disorder due to factor V deficiencies and abnormalities: an update classification. Blood Rev 1998;12:45.
16. Ginsburg D, Nichols WC, Zivelin A, et al. Combined factors V and VIII deficiency - the solution. Haemophilia 1998;4:677.