Factor X (FX) is a Vitamin K-dependent, serine protease produced by the liver that serves pivotal role as the first enzyme in the so-called common pathway of coagulation cascade in fibrin formation. Inherited FX deficiency is a rare autosomal recessive bleeding disorder that is found in 1:1,000,000 individuals. Classification of severity is based on FX coagulant activity. Specific FX replacement product is not yet readily available, but fresh frozen plasma (FFP) and prothrombin complex concentrates can be used for treatment of bleeding symptoms and preparation for surgery. Here, we reemphasize the approach to a patient with severe FX deficiency, who had a successful pregnancy outcome through the rationale use of FFP
Twelve women with severe Factor XII (FXII) deficiency were under observation for an average period o...
Congenital Factor XIII (FXIII) deficiency is a rare, inherited, autosomal recessive coagulation diso...
Factor XI deficiency (FXI) is the third most common coagulation factor deficiency after hemophilia A...
Objective: Rare co-existance of disease or pathology Background: Congenital factor X deficiency is ...
produced serine protease that serves a pivotal role in coagulation as the first enzyme in the common...
Dear Editor, Congenital factor X (FX) deficiency is an extremely rare, autosomal recessive inherited...
Introduction: Maintaining haemostasis in surgery is challenging for hereditary rare bleeding disorde...
Essentials Inherited factor XIII deficiency is a very rare bleeding disorder. We used recombinant fa...
Background: Factor X (FX) deficiency is a serious, rare bleeding disorder, with 1 in 500 000 affecte...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
Introduction: Inherited deficiencies in the coagulation pathway provide diversified models to invest...
Introduction: Factor XIII deficiency is an extremely rare type among bleeding diathesis. In factor X...
Introduction: Hereditary factor X (FX) deficiency is a rare bleeding disorder affecting 1: 500 000 t...
Acquired factor X (FX) deficiency is a rare but serious complication of primary amyloidosis, presuma...
BackgroundActivated factor X (FXa) is a vitamin K-dependent serine protease that plays a pivotal rol...
Twelve women with severe Factor XII (FXII) deficiency were under observation for an average period o...
Congenital Factor XIII (FXIII) deficiency is a rare, inherited, autosomal recessive coagulation diso...
Factor XI deficiency (FXI) is the third most common coagulation factor deficiency after hemophilia A...
Objective: Rare co-existance of disease or pathology Background: Congenital factor X deficiency is ...
produced serine protease that serves a pivotal role in coagulation as the first enzyme in the common...
Dear Editor, Congenital factor X (FX) deficiency is an extremely rare, autosomal recessive inherited...
Introduction: Maintaining haemostasis in surgery is challenging for hereditary rare bleeding disorde...
Essentials Inherited factor XIII deficiency is a very rare bleeding disorder. We used recombinant fa...
Background: Factor X (FX) deficiency is a serious, rare bleeding disorder, with 1 in 500 000 affecte...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
Introduction: Inherited deficiencies in the coagulation pathway provide diversified models to invest...
Introduction: Factor XIII deficiency is an extremely rare type among bleeding diathesis. In factor X...
Introduction: Hereditary factor X (FX) deficiency is a rare bleeding disorder affecting 1: 500 000 t...
Acquired factor X (FX) deficiency is a rare but serious complication of primary amyloidosis, presuma...
BackgroundActivated factor X (FXa) is a vitamin K-dependent serine protease that plays a pivotal rol...
Twelve women with severe Factor XII (FXII) deficiency were under observation for an average period o...
Congenital Factor XIII (FXIII) deficiency is a rare, inherited, autosomal recessive coagulation diso...
Factor XI deficiency (FXI) is the third most common coagulation factor deficiency after hemophilia A...