Objective: Rare co-existance of disease or pathology Background: Congenital factor X deficiency is a rare inherited coagulopathy. Pregnancies in women with this disorder are often associated with adverse outcomes, including miscarriage, premature labor, and hemorrhage during pregnancy and in the peripartum period. The literature on this disorder is sparse and shows a limited number of successful pregnancies in women with factor X deficiency. Case Report: In this report, we present the case of a successful pregnancy and term delivery by elective cesarean section in a 39-year-old primigravida with congenital factor X deficiency. Medical management followed the recommendations of an interdisciplinary team comprising specialists in obste...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
Inherited combined factor V and factor VIII deficiency (F5F8D) is autosomal recessive transmission d...
Factor X deficiency is a rare, autosomal recessive disorder that involves the coagulation cascade. P...
Objective: Rare co-existance of disease or pathology Background: Congenital factor X deficiency is ...
Factor XI deficiency is a hereditary blood coagulation disorders. Puerpera with factor XI deficiency...
Factor X (FX) is a Vitamin K-dependent, serine protease produced by the liver that serves pivotal ro...
Introduction: Factor XIII deficiency is an extremely rare type among bleeding diathesis. In factor X...
SummaryBackground and objectivesFactor XI deficiency is a rare hematologic disorder. Hemophilia C (f...
Factor XIII deficiency is a rare inherited coagulopathy. Factor XIII is the last clotting factor in ...
Pregnancies and deliveries represent important hemostatic challenges for congenital coagulation diso...
International audienceIntroduction: Congenital factor XIII deficiency is a very rare bleeding disord...
Essentials Inherited factor XIII deficiency is a very rare bleeding disorder. We used recombinant fa...
Dear Editor, Congenital factor X (FX) deficiency is an extremely rare, autosomal recessive inherited...
Factor VII (F VII) deficiency is a rare coagulation disorder inherited autosomal recessively. Accord...
Congenital deficiency of clotting factor VII (FVII) — refers to rare hemorrhagic diatheses, for whic...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
Inherited combined factor V and factor VIII deficiency (F5F8D) is autosomal recessive transmission d...
Factor X deficiency is a rare, autosomal recessive disorder that involves the coagulation cascade. P...
Objective: Rare co-existance of disease or pathology Background: Congenital factor X deficiency is ...
Factor XI deficiency is a hereditary blood coagulation disorders. Puerpera with factor XI deficiency...
Factor X (FX) is a Vitamin K-dependent, serine protease produced by the liver that serves pivotal ro...
Introduction: Factor XIII deficiency is an extremely rare type among bleeding diathesis. In factor X...
SummaryBackground and objectivesFactor XI deficiency is a rare hematologic disorder. Hemophilia C (f...
Factor XIII deficiency is a rare inherited coagulopathy. Factor XIII is the last clotting factor in ...
Pregnancies and deliveries represent important hemostatic challenges for congenital coagulation diso...
International audienceIntroduction: Congenital factor XIII deficiency is a very rare bleeding disord...
Essentials Inherited factor XIII deficiency is a very rare bleeding disorder. We used recombinant fa...
Dear Editor, Congenital factor X (FX) deficiency is an extremely rare, autosomal recessive inherited...
Factor VII (F VII) deficiency is a rare coagulation disorder inherited autosomal recessively. Accord...
Congenital deficiency of clotting factor VII (FVII) — refers to rare hemorrhagic diatheses, for whic...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
Inherited combined factor V and factor VIII deficiency (F5F8D) is autosomal recessive transmission d...
Factor X deficiency is a rare, autosomal recessive disorder that involves the coagulation cascade. P...