Homozygous Hemophilia A in a Female

Thromb Haemost 1985; 54(03): 728
DOI: 10.1055/s-0038-1660111

Letter to the Editor

Schattauer GmbH Stuttgart

P Sié

^*The Laboratoire d’Hémostase, Centre de Transfusion Sanguine, 31052 Toulouse Cedex, France

,

C Caranobe

^*The Laboratoire d’Hémostase, Centre de Transfusion Sanguine, 31052 Toulouse Cedex, France

,

M Benalioua

^**The Centre Emir Abdel Kader, Oran, Algérie

,

B Boneu

^*The Laboratoire d’Hémostase, Centre de Transfusion Sanguine, 31052 Toulouse Cedex, France

References
1 Graham JB. Mode of inheritance and current research. Handbook of hemophilia Excerpta Medica; Amsterdam: 1975. p 175-85
2 Morita H, Kagami M, Ebata Y, Yoshimura H. The occurrence of homozygous hemophilia in the female. Acta Haematol 1971; 45: 112-9
3 Joist JH, Bouhasin JD, Roodman S. Classical hemophilia A in a female. Acta Haematol 1977; 58: 94-102
4 Peake IR, Bloom AL, Giddings JC, Ludlam CA. An immunoradiometric assay for procoagulant factor VIII antigen. Results in haemophilia von Willebran’s disease and fetal plasma and serum. Br J Haematol 1979; 42: 269-81
5 Seabright M. A rapid banding technique for human chromosome. Lancet 1971; 2: 971-2
6 Graham JB, Barrow ES, Flyer P, Dawson DV, Elston RC. Identifying carriers of mild hemophilia. Br J Haematol 1980; 44: 671-8
7 Graham JB, Barrow ES, Elston RC. Lyonisation in hemophilia: a case of error in direct detection of heterozygous carriers. Ann NY Acad Sci 1975; 240: 141-6