Background: Factor X (FX) deficiency is a serious, rare bleeding disorder, with 1 in 500 000 affected people. Hemorrhages, hematuria, epistaxis, and other bleeding complications are frequent. Case Report: Now, we report a case of a well-known 77-year-old FX-deficient patient (Friuli variant, level <1%, mutation Pro 343→Ser, exon VIII) with hypertension, chronic obstructive pulmonary disease (COPD), and chronic gastritis, admitted many times to hospital due to surgical complications after aortic abdominal aneurysm (AAA) repair. Use of prothrombin complex concentrate (PCC) such as hemostatic therapy during surgeries and prophylaxis after discharge is shown in this article. Three consecutive surgeries were considered. First, endoleak postendop...
The story of factor X (FX) Friuli. Factor X Friuli was discovered in 1969 to 1970. However, the stor...
Despite many articles regarding the antihemorrhagic treatment and prophylaxis, there is a lack of ex...
Chemotherapy and splenectomy are the most frequently used treatments in cases of systemic light-chai...
Introduction: Maintaining haemostasis in surgery is challenging for hereditary rare bleeding disorde...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
produced serine protease that serves a pivotal role in coagulation as the first enzyme in the common...
Introduction: Hereditary factor X (FX) deficiency is a rare bleeding disorder affecting 1: 500 000 t...
Background The lack of an antidote against factor Xa inhibitors in case of major bleeding or need fo...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
The deficiency of fibrinogen, prothrombin, factor V (FV), FVII, FVIII, FIX, FX, FXI, and FXIII, call...
Background The lack of an antidote against factor Xa inhibitors in case of major ble...
Factor X (FX) is a Vitamin K-dependent, serine protease produced by the liver that serves pivotal ro...
Factor XI deficiency is a rare autosomally transmitted coagulopathy that is associated with a variab...
WOS: 000433166100006PubMed ID: 29545231Hereditary factor X (FX) deficiency is a rare bleeding disord...
Factor XII (FXII) deficiency is a congenital disorder inherited as an autosomal recessive condition....
The story of factor X (FX) Friuli. Factor X Friuli was discovered in 1969 to 1970. However, the stor...
Despite many articles regarding the antihemorrhagic treatment and prophylaxis, there is a lack of ex...
Chemotherapy and splenectomy are the most frequently used treatments in cases of systemic light-chai...
Introduction: Maintaining haemostasis in surgery is challenging for hereditary rare bleeding disorde...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
produced serine protease that serves a pivotal role in coagulation as the first enzyme in the common...
Introduction: Hereditary factor X (FX) deficiency is a rare bleeding disorder affecting 1: 500 000 t...
Background The lack of an antidote against factor Xa inhibitors in case of major bleeding or need fo...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
The deficiency of fibrinogen, prothrombin, factor V (FV), FVII, FVIII, FIX, FX, FXI, and FXIII, call...
Background The lack of an antidote against factor Xa inhibitors in case of major ble...
Factor X (FX) is a Vitamin K-dependent, serine protease produced by the liver that serves pivotal ro...
Factor XI deficiency is a rare autosomally transmitted coagulopathy that is associated with a variab...
WOS: 000433166100006PubMed ID: 29545231Hereditary factor X (FX) deficiency is a rare bleeding disord...
Factor XII (FXII) deficiency is a congenital disorder inherited as an autosomal recessive condition....
The story of factor X (FX) Friuli. Factor X Friuli was discovered in 1969 to 1970. However, the stor...
Despite many articles regarding the antihemorrhagic treatment and prophylaxis, there is a lack of ex...
Chemotherapy and splenectomy are the most frequently used treatments in cases of systemic light-chai...