Essentials Inherited factor XIII deficiency is a very rare bleeding disorder. We used recombinant factor XIII-A in a pregnant patient with factor XIII-A subunit deficiency. The patient had a successful pregnancy outcome with no pregnancy related complications. The dose of recombinant factor XIII-A was minimized by using frequent trough level monitoring. Summary: Inherited factor\ua0XIII deficiency is a very rare bleeding disorder, and is one of the causes of recurrent pregnancy loss. The use of plasma-derived FXIII to improve pregnancy outcomes has been reported. We report a 26-year-old woman with FXIII A-subunit (FXIII-A) deficiency who was treated with recombinant FXIII-A and had a successful pregnancy outcome with no pregnancy-related co...
Factor XIII deficiency is a rare bleeding disor-der that occurs in approximately 1 in 2 million pers...
With 473 patients, Iran has about one third of the world�s patients with severe congenital factor ...
Coagulation factor XIII (FXIII) exists as heterotetramer (FXIII-A(2)B(2)) in the plasma and as dimer...
Congenital Factor XIII (FXIII) deficiency is a rare, inherited, autosomal recessive coagulation diso...
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...
Coagulation factor XIII (FXIII) has a major role in the final stage of blood coagulation, is im-port...
Introduction: Hereditary Factor XIII (FXIII) deficiency is a rare autosomal recessive hemostatic dis...
BACKGROUND: The use of monthly recombinant factor XIII (rFXIII) recently demonstrated favorable sa...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
Factor XIII deficiency may be inherited or acquired. Inherited deficiency is associated with signs a...
Background: Factor XIII (FXIII) deficiency is a bleeding disorder and it inherited in an autosomal r...
Factor XIII deficiency is a rare bleeding disor-der that occurs in approximately 1 in 2 million pers...
With 473 patients, Iran has about one third of the world�s patients with severe congenital factor ...
Coagulation factor XIII (FXIII) exists as heterotetramer (FXIII-A(2)B(2)) in the plasma and as dimer...
Congenital Factor XIII (FXIII) deficiency is a rare, inherited, autosomal recessive coagulation diso...
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...
Coagulation factor XIII (FXIII) has a major role in the final stage of blood coagulation, is im-port...
Introduction: Hereditary Factor XIII (FXIII) deficiency is a rare autosomal recessive hemostatic dis...
BACKGROUND: The use of monthly recombinant factor XIII (rFXIII) recently demonstrated favorable sa...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
Factor XIII deficiency may be inherited or acquired. Inherited deficiency is associated with signs a...
Background: Factor XIII (FXIII) deficiency is a bleeding disorder and it inherited in an autosomal r...
Factor XIII deficiency is a rare bleeding disor-der that occurs in approximately 1 in 2 million pers...
With 473 patients, Iran has about one third of the world�s patients with severe congenital factor ...
Coagulation factor XIII (FXIII) exists as heterotetramer (FXIII-A(2)B(2)) in the plasma and as dimer...