Factor XII (FXII) deficiency is a congenital disorder inherited as an autosomal recessive condition. In his heterozygous form, it is relatively common in the general population. However, a total absence of FXII as seen in homozygous patients, is rare, with an incidence of approximately 1/1,000,000 individuals. Surprisingly, FXII deficiency is rather associated with thromboembolic complications. Patients do not experience a higher risk of surgical bleeding despite a markedly prolonged activated partial thromboplastin time. Given its low incidence in the general population, the finding of an unknown FXII deficiency is rare during cardiac surgery. This unique case describes a patient with an unanticipated prolonged baseline activated clotting ...
Currently available evidence supports the contention that elevated levels of factor XI (fXI) are ass...
The outcome of various surgical procedures carried out in patients with severe (homozygote) factor X...
Twenty-one patients (12 female and 9 male) with severe (homozygous) factor XII (FXII) deficiency and...
Factor XII (FXII) deficiency is a congenital disorder inherited as an autosomal recessive condition....
WOS: 000385272300025Factor XII deficiency is an important hematological problem which is characteriz...
Factor XII deficiency is an important hematological problem which is characterized by isolated prolo...
Severe Factor XI (FXI) deficiency is defined when the activated partial thromboplastin time is prolo...
Factor XII (FXII) plays a pivotal role in hemostasis, inflammation and complement system. Its defici...
Abstract Coagulation factor XII (FXII) is a plasma serine protease that belongs to the contact activ...
To investigate the occurrence of thrombotic events (myocardial infarction, deep vein thrombosis or i...
The performance of cardiopulmonary bypass (CPB) in the factor XII-deficient patient is challenging i...
Factor XII deficiency is a laboratory finding in patients who normally do not present with bleeding ...
Factor XI deficiency (FXI) is the third most common coagulation factor deficiency after hemophilia A...
Severe coagulation factor XII (FXII) deficiency is a very rare, mysterious, and not well-known inher...
We describe here the case of a 46-year-old man admitted to the emergency department (ED) and diagnos...
Currently available evidence supports the contention that elevated levels of factor XI (fXI) are ass...
The outcome of various surgical procedures carried out in patients with severe (homozygote) factor X...
Twenty-one patients (12 female and 9 male) with severe (homozygous) factor XII (FXII) deficiency and...
Factor XII (FXII) deficiency is a congenital disorder inherited as an autosomal recessive condition....
WOS: 000385272300025Factor XII deficiency is an important hematological problem which is characteriz...
Factor XII deficiency is an important hematological problem which is characterized by isolated prolo...
Severe Factor XI (FXI) deficiency is defined when the activated partial thromboplastin time is prolo...
Factor XII (FXII) plays a pivotal role in hemostasis, inflammation and complement system. Its defici...
Abstract Coagulation factor XII (FXII) is a plasma serine protease that belongs to the contact activ...
To investigate the occurrence of thrombotic events (myocardial infarction, deep vein thrombosis or i...
The performance of cardiopulmonary bypass (CPB) in the factor XII-deficient patient is challenging i...
Factor XII deficiency is a laboratory finding in patients who normally do not present with bleeding ...
Factor XI deficiency (FXI) is the third most common coagulation factor deficiency after hemophilia A...
Severe coagulation factor XII (FXII) deficiency is a very rare, mysterious, and not well-known inher...
We describe here the case of a 46-year-old man admitted to the emergency department (ED) and diagnos...
Currently available evidence supports the contention that elevated levels of factor XI (fXI) are ass...
The outcome of various surgical procedures carried out in patients with severe (homozygote) factor X...
Twenty-one patients (12 female and 9 male) with severe (homozygous) factor XII (FXII) deficiency and...