To investigate the prevalence and type of thrombotic events reported in patients with congenital factor XI (FXI) or factor VII (FVII) deficiency.Data on all patients with congenital FXI or FVII deficiency and a thrombotic event were gathered by means of a time unlimited PubMed search carried out in June 2014 and in February 2015. Appropriate keywords including the medical subject headings were used in both instances. Side tables were also consulted and cross-checking of the references was carried out to avoid omissions. The thrombosis event had to be proven by objective methods.Forty-three patients with FXI deficiency had arterial thrombosis and only eight had venous thrombosis. On the contrary, only five patients with FVII deficiency had a...
Congenital factor VII deficiency (FVIID) is a rare disorder with a wide range of bleeding manifestat...
Congenital prothrombin deficiency is one of the rarest clotting disorders. It is commonly subdivided...
Severe coagulation factor XII (FXII) deficiency is a very rare, mysterious, and not well-known inher...
Inherited factor VII (FVII) deficiency is considered to be a haemorrhagic disease. Nonetheless, some...
Background: The occurrence of a thrombotic event in congenital bleeding disorders has drawn consider...
Thrombosis in congenital factor (F) VII deficiency was investigated through extensive phenotypic and...
To investigate the occurrence of thrombotic events (myocardial infarction, deep vein thrombosis or i...
Twenty-one patients (12 female and 9 male) with severe (homozygous) factor XII (FXII) deficiency and...
Factor VII (FVII) deficiency is one of the rare inherited bleeding disorders. Thrombosis has been oc...
Objective: To investigate all cases of isolated factor VII (FVII) deficiency as gathered from person...
Factor XI (FXI) deficiency is a rare autosomal recessive disorder. Many patients with even very low ...
According to our personal experience and to the study of the literature, 11 cases of venous thrombos...
Currently available evidence supports the contention that elevated levels of factor XI (fXI) are ass...
OBJECTIVE: To investigate the incidence of thrombotic events in patients heterozygous for FXII de...
To determine whether heterozygotes with FVII deficiency have a bleeding tendency or not.Eighty-four ...
Congenital factor VII deficiency (FVIID) is a rare disorder with a wide range of bleeding manifestat...
Congenital prothrombin deficiency is one of the rarest clotting disorders. It is commonly subdivided...
Severe coagulation factor XII (FXII) deficiency is a very rare, mysterious, and not well-known inher...
Inherited factor VII (FVII) deficiency is considered to be a haemorrhagic disease. Nonetheless, some...
Background: The occurrence of a thrombotic event in congenital bleeding disorders has drawn consider...
Thrombosis in congenital factor (F) VII deficiency was investigated through extensive phenotypic and...
To investigate the occurrence of thrombotic events (myocardial infarction, deep vein thrombosis or i...
Twenty-one patients (12 female and 9 male) with severe (homozygous) factor XII (FXII) deficiency and...
Factor VII (FVII) deficiency is one of the rare inherited bleeding disorders. Thrombosis has been oc...
Objective: To investigate all cases of isolated factor VII (FVII) deficiency as gathered from person...
Factor XI (FXI) deficiency is a rare autosomal recessive disorder. Many patients with even very low ...
According to our personal experience and to the study of the literature, 11 cases of venous thrombos...
Currently available evidence supports the contention that elevated levels of factor XI (fXI) are ass...
OBJECTIVE: To investigate the incidence of thrombotic events in patients heterozygous for FXII de...
To determine whether heterozygotes with FVII deficiency have a bleeding tendency or not.Eighty-four ...
Congenital factor VII deficiency (FVIID) is a rare disorder with a wide range of bleeding manifestat...
Congenital prothrombin deficiency is one of the rarest clotting disorders. It is commonly subdivided...
Severe coagulation factor XII (FXII) deficiency is a very rare, mysterious, and not well-known inher...