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Öğe Successful Prophylactic Use of Recombinant Activated Factor VII (rFVIIa) in a Patient with Congenital FVII Deficiency and Inhibitors to FVII(WILEY, 2012) Tokgöz, H.; Çalışkan, U.; Lavigne-Lissalde, G.; Giansily-Blaizot, M.Congenital factor VII (FVII) deficiency is a rare, autosomal recessive bleeding disorder. The clinical phenotypes range from asymptomatic condition to severe disease characterized by life-threatening bleedings [1]. Optimal replacement therapy for FVII deficiency consists of recombinant activated factor VII (rFVIIa) or plasma derived FVII (pdFVII) concentrates. Although rare, the formation of neutralizing antibodies to FVII is an important concern of replacement therapy in the treatment of FVII deficiency [1]. Herein, we report the clinical progress of a patient with severe FVII deficiency who developed inhibitors against FVII during treatment with rFVIIa.Öğe Successfull Use of Prophylactic Recombinant Factor VII in a Patient with Congenital Factor VII Deficiency with Inhibitory Antibody(FERRATA STORTI FOUNDATION, 2010) Tokgöz, H.; Calışkan, U. E.[Abstract not Available]
