Acquired factor X deficiency is an extremely rare situation. It has shown to be associated with systemic amyloidosis, respiratory mycoplasma infection, factor X inhibitors, antiphospholipid antibodies, vitamin K defi ciency/liver disease as well as the use of certain medications (meropenem, valproic acid). The pathogenesis and transient nature of this deficit remain poorly understood. The authors describe the case of a teenager hospitalised for extensive burns that developed active bleeding after removal of central venous catheter. He was diagnosed with transient factor X deficiency. Normalisation of coagulation status and factor X levels occurred spontaneously 10 days after the bleeding episode
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
Factor XIII deficiency may be inherited or acquired. Inherited deficiency is associated with signs a...
Factor XII (FXII) deficiency is a congenital disorder inherited as an autosomal recessive condition....
Acquired factor X deficiency is an extremely rare situation. It has shown to be associated with syst...
Factor X deficiency is a rare, autosomal recessive disorder that involves the coagulation cascade. P...
Abstract Acquired factor X (FX) deficiency is rare, but has been reported in diverse disease states,...
Acquired factor X (FX) deficiency is a rare but serious complication of primary amyloidosis, presuma...
Congenital factor X deficiency is a rare inherited coagulation disorder, characterized by prolonged ...
A 57-year-old man developed symptoms of a respiratory tract infection which was treated with erythro...
Hemophilia due to factor VIII deficiency is most common inherited bleeding disorder in paediatric po...
During these three-years PhD we analyzed the clinical, phenotypic and molecular aspects of a rare bl...
Abstract Background Patients with extensive burns usually develop pro-coagulation soon after the inj...
Introduction: Factor XI deficiency or hemophilia C is a very rare coagulation factor deficiency, wit...
We describe a patient with a prolonged aPTT who was diagnosedas having factor XI deficiency after a ...
The spectrum of the clinical manifestations of congenital factor X deficiency was studied in 32 Iran...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
Factor XIII deficiency may be inherited or acquired. Inherited deficiency is associated with signs a...
Factor XII (FXII) deficiency is a congenital disorder inherited as an autosomal recessive condition....
Acquired factor X deficiency is an extremely rare situation. It has shown to be associated with syst...
Factor X deficiency is a rare, autosomal recessive disorder that involves the coagulation cascade. P...
Abstract Acquired factor X (FX) deficiency is rare, but has been reported in diverse disease states,...
Acquired factor X (FX) deficiency is a rare but serious complication of primary amyloidosis, presuma...
Congenital factor X deficiency is a rare inherited coagulation disorder, characterized by prolonged ...
A 57-year-old man developed symptoms of a respiratory tract infection which was treated with erythro...
Hemophilia due to factor VIII deficiency is most common inherited bleeding disorder in paediatric po...
During these three-years PhD we analyzed the clinical, phenotypic and molecular aspects of a rare bl...
Abstract Background Patients with extensive burns usually develop pro-coagulation soon after the inj...
Introduction: Factor XI deficiency or hemophilia C is a very rare coagulation factor deficiency, wit...
We describe a patient with a prolonged aPTT who was diagnosedas having factor XI deficiency after a ...
The spectrum of the clinical manifestations of congenital factor X deficiency was studied in 32 Iran...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
Factor XIII deficiency may be inherited or acquired. Inherited deficiency is associated with signs a...
Factor XII (FXII) deficiency is a congenital disorder inherited as an autosomal recessive condition....