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
Thromb Haemost 2008; 99(01): 238-239
DOI: 10.1160/TH07-08-0486
DOI: 10.1160/TH07-08-0486
Letters to the Editor
Report on a disease-adapted treatment in a patient with severe factor X deficiency resulting from a homozygous factor X gene mutation
Further Information
Correspondence to:
Rainer B. Zotz
Department of Hemostasis and Transfusion Medicine
Heinrich-Heine University Medical Center
Moorenstrasse 5, 40225 Düsseldorf, Germany
Phone: Tel.:+49 211 811 7237
Fax: +49 211 811 6221
Email: zotz@med.uni-duesseldorf.de
Publication History
Received:
02 August 2007
Accepted after major revision:
11 October 2007
Publication Date:
24 November 2017 (online)
#
-
References
- 1 Herrmann FH, Auerswald G, Ruiz-Saez A. et al. The Greifswald Factor X Deficiency Study Group. Factor X deficiency: clinical manifestation of 102 subject from Europe and Latin America with mutations in the factor 10 gene. Haemophilia 2006; 12: 479-489.
- 2 Dewerchin M, Liang Z, Moons L. et al. Blood coagulation factor X deficiency causes partial embryonic lethality and fatal neonatal bleeding in mice. Thromb Haemost 2000; 83: 185-190.
- 3 Al-Hilal A, Wulff K, Abdel-Razeq H. et al. Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyad anomaly. Thromb Haemost 2007; 97: 542-545.
- 4 Peyvandi F, Menegatti M, Santagostino E. et al. Gene mutations and three-dimensional structural analysis in 13 families with severe Factor X deficiency. Br J Haematol 2002; 117: 685-692.
- 5 Todd T, Perry DJ, Hayman E. et al. Severe factor X deficiency due to a homozygous mutation (Cys364Arg) that disrupts a disulphide bond in the catalytic domain. Haemophilia 2006; 12: 621-624.
- 6 Kohler M. Thrombogenicity of prothrombin complex concentrates. Thromb Res 1999; 95: S13-17.
Correspondence to:
Rainer B. Zotz
Department of Hemostasis and Transfusion Medicine
Heinrich-Heine University Medical Center
Moorenstrasse 5, 40225 Düsseldorf, Germany
Phone: Tel.:+49 211 811 7237
Fax: +49 211 811 6221
Email: zotz@med.uni-duesseldorf.de
-
References
- 1 Herrmann FH, Auerswald G, Ruiz-Saez A. et al. The Greifswald Factor X Deficiency Study Group. Factor X deficiency: clinical manifestation of 102 subject from Europe and Latin America with mutations in the factor 10 gene. Haemophilia 2006; 12: 479-489.
- 2 Dewerchin M, Liang Z, Moons L. et al. Blood coagulation factor X deficiency causes partial embryonic lethality and fatal neonatal bleeding in mice. Thromb Haemost 2000; 83: 185-190.
- 3 Al-Hilal A, Wulff K, Abdel-Razeq H. et al. Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyad anomaly. Thromb Haemost 2007; 97: 542-545.
- 4 Peyvandi F, Menegatti M, Santagostino E. et al. Gene mutations and three-dimensional structural analysis in 13 families with severe Factor X deficiency. Br J Haematol 2002; 117: 685-692.
- 5 Todd T, Perry DJ, Hayman E. et al. Severe factor X deficiency due to a homozygous mutation (Cys364Arg) that disrupts a disulphide bond in the catalytic domain. Haemophilia 2006; 12: 621-624.
- 6 Kohler M. Thrombogenicity of prothrombin complex concentrates. Thromb Res 1999; 95: S13-17.