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Thromb Haemost 2001; 86(04): 1131
DOI: 10.1055/s-0037-1616554
DOI: 10.1055/s-0037-1616554
Letters to the Editor
Congenital Deficiency of Vitamin K Dependent Coagulation Factors – Its Rarity and Need for an International Registry
Further Information
Publication History
Received
12 January 2001
Accepted after revision
16 March 2001
Publication Date:
09 December 2017 (online)
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References
- 1 Oldenburg J, Von Brederlow B, Fregin A, Rost S, Walz W, Ebeel W. et al. Congenital deficiency of vitamin K dependent coagulation factor in two families presents as a genetic defect of the vitamin K epoxide reductase complex. Thromb Haemost 2000; 84: 937-41.
- 2 Ghosh K, Shetty S, Mohanty D. Inherited deficiency of multiple vitamin K dependent coagulation factors and coagulation inhibitors presenting as haemorrhagic diathesis, mental retardation and growth retardation. Am J Haematol 1996; 52: 67.
- 3 Bonch A, Barziv J. Hereditary deficiency of vitamin K dependent coagulation factors with skeletal abnormalities. Am J Med Genet 1996; 65: 241-3.
- 4 Brenner B. Hereditary deficiency of vitamin K dependent coagulation factors. Thromb Haemost 2000; 84: 935-6.
- 5 Johnson CA, Chung KS, McGrath KM, Bean PE, Roberts HR. Characterization of a variant prothrombin in a patient congenitally deficient in factors II, VII, IX and X. Br J Haematol 1980; 44: 461-5.
- 6 Spronk HM, Farah RA, Buchanan GR, Vermeer C, Soute BA. Novel mutation in the gamma-glutamyl carboxylase gene resulting in congenital combined deficiency of all vitamin K dependent blood coagulation factors. Blood 2000; 96: 3650-2.