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About 518 results

ALLMedicine™ Factor VII Deficiency Center

Research & Reviews  253 results

Identification of two novel mutations in three children with congenital factor VII defi...
https://doi.org/10.1097/MBC.0000000000001022
Blood Coagulation & Fibrinolysis : an International Journ... Liang K, Nikuze L et. al.

Feb 15th, 2021 - Congenital factor VII deficiency (FVIID) is a rare F7 gene mutation causing bleeding disorder inherited in an autosomal recessive manner. In this study, we aimed to identify genetic defects and analyze their relationships with phenotype in three C...

Compound Heterozygous Mutations in the F7 Gene in 2 Unrelated Families With Congenital ...
https://doi.org/10.1097/MPH.0000000000002057
Journal of Pediatric Hematology/oncology; Ma C, Wang Y et. al.

Jan 22nd, 2021 - Factor VII (FVII) deficiency is a rare bleeding disorder normally caused by homozygous and compound heterozygous mutations in the F7 gene. Whole-exome sequencing was performed to identify F7 mutations in 3 individuals from 2 unrelated families who...

Management of pregnancy in women with factor VII deficiency: A case series.
https://doi.org/10.1111/hae.14086
Haemophilia : the Official Journal of the World Federatio... Lee EJ, Burey L et. al.

Jun 26th, 2020 - Inherited factor VII deficiency is the most common autosomal recessive inherited bleeding disorder, with an estimated incidence of one per 500 000 cases in the general population. Bleeding manifestations correlate poorly with circulating FVII leve...

Factor VII Deficiency in Patients Receiving Chronic Packed Cell Transfusions.
https://doi.org/10.1097/MPH.0000000000001854
Journal of Pediatric Hematology/oncology; Abu-Quider A, Asleh M et. al.

Jun 10th, 2020 - Acquired factor VII deficiency is a rare coagulopathy that has not been reported in transfusion-dependent patients so far. In this study, we reviewed files of 26 transfusion-dependent patients for coagulation profiles, factor V levels, factor VII ...

Successful Splenectomy Management in a Patient With Moderate Factor VII Deficiency and ...
https://doi.org/10.1097/MPH.0000000000001738
Journal of Pediatric Hematology/oncology; Goudarzipour K, Amiri V et. al.

Feb 7th, 2020 - By the advent of the effective therapies for many coagulation diseases and hereditary spherocytosis (HS), patient's survival has been improved significantly; however, if patients are diagnosed late or left untreated, both diseases could ominously ...

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Drugs  3 results see all →

Clinicaltrials.gov  261 results

Identification of two novel mutations in three children with congenital factor VII defi...
https://doi.org/10.1097/MBC.0000000000001022
Blood Coagulation & Fibrinolysis : an International Journ... Liang K, Nikuze L et. al.

Feb 15th, 2021 - Congenital factor VII deficiency (FVIID) is a rare F7 gene mutation causing bleeding disorder inherited in an autosomal recessive manner. In this study, we aimed to identify genetic defects and analyze their relationships with phenotype in three C...

Profilnine - factor ix complex kit-GRIFOLS USA, LLC
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=79821042-86a5-4a64-b621-76de0a0bbab2

Jan 31st, 2021 - Profilnine, Factor IX Complex, is indicated for the prevention and control of bleeding in patients with factor IX deficiency (hemophilia B). Profilnine contains non-therapeutic levels of factor VII and is not indicated for use in the treatment of ...

Compound Heterozygous Mutations in the F7 Gene in 2 Unrelated Families With Congenital ...
https://doi.org/10.1097/MPH.0000000000002057
Journal of Pediatric Hematology/oncology; Ma C, Wang Y et. al.

Jan 22nd, 2021 - Factor VII (FVII) deficiency is a rare bleeding disorder normally caused by homozygous and compound heterozygous mutations in the F7 gene. Whole-exome sequencing was performed to identify F7 mutations in 3 individuals from 2 unrelated families who...

Management of pregnancy in women with factor VII deficiency: A case series.
https://doi.org/10.1111/hae.14086
Haemophilia : the Official Journal of the World Federatio... Lee EJ, Burey L et. al.

Jun 26th, 2020 - Inherited factor VII deficiency is the most common autosomal recessive inherited bleeding disorder, with an estimated incidence of one per 500 000 cases in the general population. Bleeding manifestations correlate poorly with circulating FVII leve...

Factor VII Deficiency in Patients Receiving Chronic Packed Cell Transfusions.
https://doi.org/10.1097/MPH.0000000000001854
Journal of Pediatric Hematology/oncology; Abu-Quider A, Asleh M et. al.

Jun 10th, 2020 - Acquired factor VII deficiency is a rare coagulopathy that has not been reported in transfusion-dependent patients so far. In this study, we reviewed files of 26 transfusion-dependent patients for coagulation profiles, factor V levels, factor VII ...

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News  1 results

Clotting Factor Disappoints for Intracerebral Hemorrhage
https://www.medpagetoday.com/cardiology/strokes/9454

May 14th, 2008 - Action Points Explain to interested patients that there are no proven treatments for intracerebral hemorrhage. Note that rFVIIa is FDA approved for treatment of bleeding and prevention of bleeding during invasive procedures in patients who have he...

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