Intracranial hemorrhage (ICH) is a medical emergency. In congenital bleeding disorders, ICH is a devastating presentation accompanied with a high rate of morbidity and mortality. The prevalence of ICH is highly variable among congenital bleeding disorders, with the highest incidence observed in factor (F) XIII deficiency (FXIIID) (�30). This life-threatening presentation is less common in afibrinogenemia, FVIII, FIX, FVII, and FX deficiencies, and is rare in severe FV and FII deficiencies, type 3 von Willebrand disease and inherited platelet function disorders (IPFDs). In FXIIID, this diathesis most often occurs after trauma in children, whereas spontaneous ICH is more frequent in adults. About 15 of patients with FXIIID and ICH die; the ...
Based on the description of a severe bleeding disorder in a young child a short overview on the gene...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
Intracranial hemorrhage (ICH) is a medical emergency. In congenital bleeding disorders, ICH is a dev...
Intracranial hemorrhage (ICH), as a life-Threatening bleeding among all kinds of congenital bleeding...
Intracranial hemorrhage (ICH), as a life-Threatening bleeding among all kinds of congenital bleeding...
Background Intracranial hemorrhage (ICH) is a life-threatening situation in childhood. Congenital fa...
Background Intracranial hemorrhage (ICH) is a life-threatening situation in childhood. Congenital fa...
With 473 patients, Iran has about one third of the world�s patients with severe congenital factor ...
Background: Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder, which has the hig...
Background: Factor XIII (FXIII) deficiency is a bleeding disorder and it inherited in an autosomal r...
Congenital factor XIII (FXIII) deficiency is a rare coagulopathy with the highest incidence in Iran....
Introduction: Hereditary Factor XIII (FXIII) deficiency is a rare autosomal recessive hemostatic dis...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
Based on the description of a severe bleeding disorder in a young child a short overview on the gene...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
Intracranial hemorrhage (ICH) is a medical emergency. In congenital bleeding disorders, ICH is a dev...
Intracranial hemorrhage (ICH), as a life-Threatening bleeding among all kinds of congenital bleeding...
Intracranial hemorrhage (ICH), as a life-Threatening bleeding among all kinds of congenital bleeding...
Background Intracranial hemorrhage (ICH) is a life-threatening situation in childhood. Congenital fa...
Background Intracranial hemorrhage (ICH) is a life-threatening situation in childhood. Congenital fa...
With 473 patients, Iran has about one third of the world�s patients with severe congenital factor ...
Background: Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder, which has the hig...
Background: Factor XIII (FXIII) deficiency is a bleeding disorder and it inherited in an autosomal r...
Congenital factor XIII (FXIII) deficiency is a rare coagulopathy with the highest incidence in Iran....
Introduction: Hereditary Factor XIII (FXIII) deficiency is a rare autosomal recessive hemostatic dis...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
Based on the description of a severe bleeding disorder in a young child a short overview on the gene...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...
International audienceThis FranceCoag network study assessed 33 patients with congenital factor XIII...