Congenital afibrinogenemia: from etiopathogenesis to challenging clinical management.

Abstract excerpt

INTRODUCTION: Congenital afibrinogenemia belongs to the group of autosomal recessive bleeding disorders and represents the absolute deficiency of fibrinogen detected by an antigenic test. This can lead to severe clinical manifestations of the disorder. Therefore, it is very important to take afibrinogenemia into account in the process of the differential diagnostics of the patients. AREAS COVERED: The authors...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Afibrinogenemia
• Share to Blood Coagulation Tests
• Share to Disease Management