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Von Willebrand hastalığı’nda oral cerrahi yaklaşım: olgu sunumu
2008
Journal:  
Cumhuriyet Dental Journal
Author:  
Abstract:

Von Willebrand Disease (VWD) is a hereditary coagulation disorder characterized by a deficient or abnormal plasma protein known as the von Willebrand factor (vWF). Patients with VWD usually manifest a dual hemostatic defect characterized by a prolonged bleeding time and low plasma levels of Factor VIII coagulant activity. In the present case, management of 39 years old female patient with VWD in whom cryoprecipitate transfusion was applied for multiple tooth extractions was reported and alternative treatment protocols were discussed. ÖZET Von Willebrand Hastalığı (VWH), von Willebrand faktör (vWF) olarak bilinen plazma proteinin yetersiz ya da anormal şekilde bulunması ile karakterize herediter koagülasyon bozukluğudur. VWH olan hastalar, genellikle uzamış kanama zamanı ve Faktör VIII koagülasyon aktivitesinin düşük plazma değerleri ile karakterize ikili  bir hemostatik defekte sahiptirler. Bu olgu raporunda, kliniğimize VWH tanısı ile başvuran 39 yaşındaki bayan hastanın, kriyospitat replasman tedavisi ile çoklu diş çekimleri gerçekleştirilip, alternatif tedavi protokolleri tartışılmıştır. Anahtar kelimeler: Von Willebrand Hastalığı, diş çekimi

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Oral Surgery Approach to Von Willebrand's Disease: Facts Presentation
2008
Author:  
Abstract:

Von Willebrand Disease (VWD) is a hereditary coagulation disorder characterized by a deficient or abnormal plasma protein known as the von Willebrand factor (vWF). Patients with VWD usually manifest a dual hemostatic defect characterized by a prolonged bleeding time and low plasma levels of Factor VIII coagulant activity. In the present case, management of 39 years old female patient with VWD in whom cryoprecipitate transfusion was applied for multiple tooth extractions was and alternative treatment protocols were discussed. Von Willebrand Disease (VWH) is a hereditary coagulation disorder characterized by the insufficient or abnormal presence of plasma protein known as von Willebrand factor (vWF). Patients with VWH usually have a binary hemostatic defect characterized by prolonged bleeding time and low plasma values of factor VIII coagulation activity. In this incident report, the 39-year-old female patient, who applied to our clinic with a VWH diagnosis, performed multiple tooth screens and discussed the protocols of alternative therapy with cryospitals replacement treatment. Keywords: Von Willebrand's Disease, Dentistry

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Cumhuriyet Dental Journal

Field :   Sağlık Bilimleri

Journal Type :   Uluslararası

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Cumhuriyet Dental Journal