Factor XIII deficiency is a rare inherited coagulopathy. Factor XIII is the last clotting factor in the coagulation cascade to insure strength and stability to fibrin clots. Without this enzyme, the fibrous clot is unstable and nonresistant to fibrinolysis. Gravid women with this congenital disease are especially at risk for complications including miscarriages and hemorrhage without appropriate interventions. We present a case of a woman in her 20s with Factor XIII deficiency who was treated with cryoprecipitate and had a successful normal spontaneous vaginal delivery; subsequently, patient suffered from postpartum hemorrhage and consumptive coagulopathy due to consumption of Factor XIII, requiring emergency surgical intervention. Intraope...
Factor XIII deficiency may be inherited or acquired. Inherited deficiency is associated with signs a...
Introduction Factor XIII deficiency is a relatively rare hereditary bleeding disorder, whi...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
Introduction: Factor XIII deficiency is an extremely rare type among bleeding diathesis. In factor X...
International audienceIntroduction: Congenital factor XIII deficiency is a very rare bleeding disord...
Introduction: Hereditary Factor XIII (FXIII) deficiency is a rare autosomal recessive hemostatic dis...
Objective: Rare co-existance of disease or pathology Background: Congenital factor X deficiency is ...
Postpartum hemorrhage (PPH) is a major cause of maternal mortality, which is a common clinical manif...
Essentials Inherited factor XIII deficiency is a very rare bleeding disorder. We used recombinant fa...
Congenital Factor XIII (FXIII) deficiency is a rare, inherited, autosomal recessive coagulation diso...
Factor XI deficiency is a hereditary blood coagulation disorders. Puerpera with factor XI deficiency...
Copyright © 2013 Akio Kanda et al. This is an open access article distributed under the Creative Com...
A Caucasian male infant born full term via normal spontaneous vaginal delivery was given vitamin K a...
Factor XIII deficiency may be inherited or acquired. Inherited deficiency is associated with signs a...
Introduction Factor XIII deficiency is a relatively rare hereditary bleeding disorder, whi...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
Introduction: Factor XIII deficiency is an extremely rare type among bleeding diathesis. In factor X...
International audienceIntroduction: Congenital factor XIII deficiency is a very rare bleeding disord...
Introduction: Hereditary Factor XIII (FXIII) deficiency is a rare autosomal recessive hemostatic dis...
Objective: Rare co-existance of disease or pathology Background: Congenital factor X deficiency is ...
Postpartum hemorrhage (PPH) is a major cause of maternal mortality, which is a common clinical manif...
Essentials Inherited factor XIII deficiency is a very rare bleeding disorder. We used recombinant fa...
Congenital Factor XIII (FXIII) deficiency is a rare, inherited, autosomal recessive coagulation diso...
Factor XI deficiency is a hereditary blood coagulation disorders. Puerpera with factor XI deficiency...
Copyright © 2013 Akio Kanda et al. This is an open access article distributed under the Creative Com...
A Caucasian male infant born full term via normal spontaneous vaginal delivery was given vitamin K a...
Factor XIII deficiency may be inherited or acquired. Inherited deficiency is associated with signs a...
Introduction Factor XIII deficiency is a relatively rare hereditary bleeding disorder, whi...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...