RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00035024.xml
Thromb Haemost 2006; 95(05): 896-897
DOI: 10.1160/TH06-01-0055
DOI: 10.1160/TH06-01-0055
Case Report
Successful pregnancy in a patient with factor V deficiency: Case report and review of the literature
Weitere Informationen
Publikationsverlauf
Received
27. Januar 2006
Accepted after resubmission
07. März 2006
Publikationsdatum:
01. Dezember 2017 (online)
-
References
- 1 Nolf P. Contribution à l’étude de la coagulation du sang. Les facteurs primordiaux, leurs origine. Arch Int Physiol 1908; 06: 1-72.
- 2 Owren PA. Parahaemophilia, haemorrhagic diathesis due to the absence of a previously unknown clotting factor. Lancet 1947; 01: 446-8.
- 3 Bolton-Maggs PHB, Perry DJ, Chalmers EA. et al. The rare coagulation disorders– review with guidelines for management from the United kingdom Haemophilia Centre Doctors’ Organisation, Haemophilia. 2004; 10: 593-628.
- 4 Sun H, Yang TL, Yang A. et al. The murine platelet and plasma factor V pools are biosynthetically distinct and sufficient for minimal hemostasis. Blood 2003; 102: 2856-61.
- 5 Guasch JF, Cannegieter S, Reitsma PH. et al. Severe coagulation factor V deficiency caused by a 4 bp deletion in the factor V gene. Br J Haematol 1998; 101: 32-9.
- 6 Peyvandi E, Manucci PM. Rare coagulation disorders. Thromb Haemost 1999; 82: 1207-14.
- 7 Girolami A, Scarano L, Girolami B. et al. Hemorrhagic and thrombotic disorders due to factor V deficiencies and abnormalities: an updated classification. Blood Rev 1998; 12: 45-51.
- 8 Lak M, Sharfian R, Peyvandi F. et al. Symptoms of inherited factor V deficiency in 35 Iranian patients. Br J Thromb Haemost 1998; 83: 1067-71.
- 9 Mann KG. How much factor V is enough?. Thromb Haemost 2000; 83: 3-4.
- 10 Field JB, Ware AG. Studies in parahaemophilia. J Clin Invest 1954; 33: 932.
- 11 Fajardo LF, Silvert D. Pregnancy and Ac-globulin deficiency. Report of a case. Am J Obstet gynaecol 1957; 74: 909-19.
- 12 Melliger EJ, Duckert F. Major surgery ina subject with factor V deficiency. Cholecystectomy in a parahaemophilic woman and review of the literature. Thromb Diath Haemor 1971; 25: 438-46.
- 13 Langer R, Caspi E, Kaufman S. et al. Management of labor in a patient with factor V deficiency. Isr J Med Sci 1982; 18: 701-3.
- 14 Brink AJ, Kingsley CS. A familial disorder of blood coagulation due to deficiency if the labile factor. Q J Med 1952; 21: 19-31.
- 15 Stohlman F, Harrington WJ, Molony WC. Parahaemophilia (Owren’s disease); report of a case in a woman with studies on other members of her family. J Lab Clin Med 1952; 38: 842-5.
- 16 Noia G, De Carolis S, De Stefano V. et al. Factor V deficiency in pregnancy complicated by Rh immunization and placenta previa.A case report and a review of the literature. Acta Obstet Gynecol Scand 1997; 76: 890-2.
- 17 Phillips LL, Little WA. Factor V deficiency in obstetrics. Obstet Gynecol 1962; 19: 507-12.
- 18 O’Connell MP, Eogan M, Murphy KM. et al. Solvent-detergent plasma as replacement therapy in a pregnant patient with factor V deficiency. J Matern Fetal Neonatal Med 2004; 16: 69-70.
- 19 Girolami A, Scandellari R, Lombardi AM. et al. Pregnancy and oral contraceptives in factor V deficiency:a study of 22 patients (five homozygotes and 17 heterozygotes) and a review of the literature. Haemophilia 2005; 11: 26-30.
- 20 Caldwell DC, Williamson RA, Goldsmith JC. Hereditary coagulopathies in pregnancy. Clin Obstet Gynecol 1985; 28: 53-72.
- 21 Van Wijk R, Nieuwenhuis K, Van den Berg M. et al. Five novel mutations in the gene for human blood coagulation factor V associated with type 1 factor V deficiency. Blood 2001; 98: 358-67.
- 22 Montefusco MC, Duga S, Asselta R. et al. Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutations. Blood 2003; 102: 3210-6.
- 23 Peyvandi F, Duga S, Akhavan S. et al. Rare coagulation deficiencies. Haemophilia 2002; 08: 308-21.
- 24 Van Wijk R, Montefusco MC, Duga F. et al. Coexistence of a novel homozygous nonsense mutation in exon 13 of the factor v gene with the homozygous Leiden mutation in two unrelated patients with severe factor V deficiency. Br J Haematol 2001; 114: 871-4.