Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00035024.xml
Download PDF
Thromb Haemost 2011; 106(01): 180-181
DOI: 10.1160/TH10-11-0732
DOI: 10.1160/TH10-11-0732
Letters to the Editor
Congenital combined deficiency of factor VII and X in a patient due to accidental diphacinone intoxication
Authors
Further Information
Publication History
Received: 16 November 2010
Accepted after major revision: 15 April 2011
Publication Date:
24 November 2017 (online)
-
References
- 1 Mariani G, Herrmann FH, Dolce A. et al. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thromb Haemost 2005; 93: 481-487.
- 2 Uprichard J, Perry DJ. Factor X deficiency. Blood Rev 2002; 16: 97-110.
- 3 Girolami A, Ruzzon E, Tezza F. et al. Congenital combined defects of factor VII: a critical review. Acta Haematol 2007; 117: 51-56.
- 4 Girolami A, Ruzzon E, Tezza F. et al. Congenital FX deficiency combined with other clotting defects or with other abnormalities: a critical evaluation of the literature. Haemophilia 2008; 14: 323-328.
- 5 Boxus G, Slacmeulder M, Ninane J. Combined hereditary deficiency in factors VII and X revealed by a prolonged partial thromboplastin time. Arch Pedi- atr 1997; 4: 44-47.
- 6 Menegatti M, Karimi M, Garagiola I. et al. A rare inherited coagulation disorder: combined homozygous factor VII and factor X deficiency. Am J Hema-tol 2004; 77: 90-91.
- 7 Pfeiffer RA, Ott R, Gilgenkrantz S. et al. Deficiencyof coagulation factors VII and X associated withdeletion of a chromosome 13 (q34). Evidence fromtwo cases with 46,XY,t(13; Y)(q11; q34). HumGenet 1982; 62: 358-360.
- 8 Ott R, Pfeiffer RA. Evidence that activities of coagu-lation factors VII and X are linked to chromosome13 (q34). Hum Hered 1984; 34: 123-126.
- 9 Peyvandi F, Jenkins PV, Mannucci PM. et al. Molec-ular characterisation and three-dimensional struc-tural analysis of mutations in 21 unrelated familieswith inherited factor VII deficiency. Thromb Hae-most 2000; 84: 250-257.
- 10 Peyvandi F, Garagiola I, Palla R. et al. Role of the 2adenine (g.11293_11294insAA) insertion poly-morphism in the 3’ untranslated region of the fac-tor VII (FVII) gene: molecular characterization of apatient with severe FVII deficiency. Hum Mutat 2005; 26: 455-461.
- 11 Herrmann FH, Wulff K, Auerswald G. et al. FactorVII deficiency: Clinical manifestation of 717 subjects from Europe and Latin America with mu-tations in the factor 7 gene. Haemophilia 2009; 15: 267-280.
- 12 Pinotti M, Camire RM, Baroni M. et al. Impaired prothrombinase activity of factor X Gly381Asp results in severe familial CRM+ FX deficiency. Thromb Haemost 2003; Feb 89: 243-248.
- 13 Ren P, Stark PY, Johnson RL. et al. Mechanism of action of anticoagulants: correlation between the inhibition of prothrombin synthesis and the regeneration of vitamin Kj from vitamin Kj epoxide. J Pharmacol Exp Ther 1977; 201: 541-546.
- 14 Watt BE, Proudfoot AT, Bradberry SM. et al. Anticoagulant rodenticides. Toxicol Rev 2005; 24: 259-269.
- 15 Murphy MJ. Rodenticides. Vet Clin North Am Small Anim Pract 2002; 32: 469-484.