Congenital afibrinogenemia in a newborn

Congenital afibrinogenemia in a newborn

Introduction: Congenital afibrinogenemia is a rare coagulation disorder characterized by a deficiency in the fibrinogen molecule. Fibrinogen is a hexameric glycoprotein consisting of a polypeptide chain encoded by FGB, FGA, and FGG and is required for normal hemostasis. Changes in FGA, FGB, and FGG...

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Bibliographic Details
Main Authors: Özay Mustafa, Kara Mustafa, Keskin Zuhal
Format: Article
Language:English
Published: Association of medical doctors Sanamed Novi Pazar 2022-12-01
Series:Sanamed
Subjects:
congenital afibrinogenemia
fibrinogen beta chain
newborn
Online Access:https://www.sanamed.rs/OJS/index.php/Sanamed/article/view/560/311

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