Klinik: 

Definition: Erbliche Erkrankungen mit einer erhöhten Blutungsneigung, die auf Störungen der Gerinnungsfaktoren zurückzuführen sind, wurden in dieser Gruppe zusammengefasst.

Literatur: 

Fuse I et al. (1996) Disorders of platelet function.
Bick R et al. (2001) Vascular thrombohemorrhagic disorders: hereditary and acquired.
Triplett DA et al. (2000) Coagulation and bleeding disorders: review and update.
Santagostino E et al. (2000) Guidelines on replacement therapy for haemophilia and inherited coagulation disorders in Italy.
Nitu-Whalley IC et al. (1999) Acquired von Willebrand syndrome--report of 10 cases and review of the literature.
Baker WF et al. (1999) Treatment of hereditary and acquired thrombophilic disorders.
Basi DL et al. (1999) Bleeding and coagulation problems in the dental patient. Hereditary disease and medication-induced risks.
Roberts HR et al. (2004) Current concepts of hemostasis: implications for therapy.
Ramasamy I et al. (2004) Inherited bleeding disorders: disorders of platelet adhesion and aggregation.
Srivastava A et al. (2005) von Willebrand disease in the developing world.
Asselta R et al. (2006) The molecular basis of quantitative fibrinogen disorders.
Peyvandi F et al. (2006) Genetic diagnosis of haemophilia and other inherited bleeding disorders.
Franchini M et al. (2007) Prophylaxis in von Willebrand disease.
Dargaud Y et al. (2007) Haemophilia therapies.
Rodgers GM et al. (2009) Role of antithrombin concentrate in treatment of hereditary antithrombin deficiency. An update.
Hill M et al. (2008) Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias.