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...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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Association of medical doctors Sanamed Novi Pazar
2022-12-01
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| Series: | Sanamed |
| Subjects: | |
| Online Access: | https://www.sanamed.rs/OJS/index.php/Sanamed/article/view/560/311 |