This study presents the demographics, clinical spectrum, and outcome of patients with congenital factor VII (FVII) deficiency at a tertiary care center over a period of 12 years. Of the 49 patients, 27 (55%) patients were males. Consanguinity was found in 92% of the patients. The median age of symptom onset was 2.4 (interquartile range [IQR]: 1.1-6.5) years with a median age of 5.8 (IQR: 3.1-10) years at diagnosis. Life-threatening complications like intracranial bleeding (ICB) and intra-abdominal bleeding (IAB) were observed in 8 (16.4%) patients. We found that 11 (55%) of the 20 patients with FVII coagulant activity (FVIIc) 5% were affected by severe symptoms. Age (P = .042; odds ratio 6.46). Overall, 4 (8.2%) died as a consequence of ICB...
Congenital factor VII deficiency is the most common form of rare coagulation factor deficiencies. Th...
Factor VII deficiency is one of the \u27rare inherited disorders of coagulation.\u27 Few cases of Fa...
We have studied the molecular basis of factor (F) VII deficiency in 11 unrelated Indian patients. Mu...
Congenital factor VII (FVII) (proconvertin) is a rare autosomal recessive bleeding disorder. Bleedin...
Factor VII (FVII) deficiency is one of the rare inherited bleeding disorders. Thrombosis has been oc...
International audienceInherited factor VII (FVII) deficiency is one of the commonest rare bleeding d...
Summary. Factor VII (FVII) deficiency is the most frequent among rare congenital bleeding disorders,...
Shilpa Jain,1,2 Jennifer Donkin,3 Mary-Jane Frey,4 Skye Peltier,5 Sriya Gunawardena,6 David L Cooper...
Inherited factor VII (FVII) deficiency is a rare autosomal recessive hemorrhagic disorder. Clinical ...
International audienceINTRODUCTION:A paucity of data exists on the incidence, diagnosis and treatmen...
: Congenital factor VII (FVII) deficiency is a rare bleeding disorder with an estimated prevalence o...
Factor VII deficiency and factor X deficiency and very rare disorders individually. Combined Factor ...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
To investigate the relationship between clinical phenotype, clotting activity (FVIIc) and FVII genot...
Congenital factor VII deficiency is the most common form of rare coagulation factor deficiencies. Th...
Factor VII deficiency is one of the \u27rare inherited disorders of coagulation.\u27 Few cases of Fa...
We have studied the molecular basis of factor (F) VII deficiency in 11 unrelated Indian patients. Mu...
Congenital factor VII (FVII) (proconvertin) is a rare autosomal recessive bleeding disorder. Bleedin...
Factor VII (FVII) deficiency is one of the rare inherited bleeding disorders. Thrombosis has been oc...
International audienceInherited factor VII (FVII) deficiency is one of the commonest rare bleeding d...
Summary. Factor VII (FVII) deficiency is the most frequent among rare congenital bleeding disorders,...
Shilpa Jain,1,2 Jennifer Donkin,3 Mary-Jane Frey,4 Skye Peltier,5 Sriya Gunawardena,6 David L Cooper...
Inherited factor VII (FVII) deficiency is a rare autosomal recessive hemorrhagic disorder. Clinical ...
International audienceINTRODUCTION:A paucity of data exists on the incidence, diagnosis and treatmen...
: Congenital factor VII (FVII) deficiency is a rare bleeding disorder with an estimated prevalence o...
Factor VII deficiency and factor X deficiency and very rare disorders individually. Combined Factor ...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
The complex formed between the procoagulant serine protease activated factor VII (FVII) and the memb...
To investigate the relationship between clinical phenotype, clotting activity (FVIIc) and FVII genot...
Congenital factor VII deficiency is the most common form of rare coagulation factor deficiencies. Th...
Factor VII deficiency is one of the \u27rare inherited disorders of coagulation.\u27 Few cases of Fa...
We have studied the molecular basis of factor (F) VII deficiency in 11 unrelated Indian patients. Mu...