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Afibrinogenemia
- Congenital afibrinogenemia is a bleeding disorder caused by impairment of the blood clotting process. Normally, blood clots protect the body after an injury by ...
- ... person will have a complete lack of fibrinogen (afibrinogenemia). When the abnormal gene is passed down from ...
- Rare Clotting Factor Deficiencies (World Federation of Hemophilia)Bleeding Disorders/Specifics ... Bleeding Disorders ... Vitamin K/Learn More ... Vitamin K ... World Federation of Hemophilia
- ... in the FGA gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... the excessive bleeding seen in people with congenital afibrinogenemia. More About This Health Condition Mutations in one ...
- ... in the FGG gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... the excessive bleeding seen in people with congenital afibrinogenemia. More About This Health Condition Mutations in one ...
- ... in the FGB gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion. Blood. 2000 Feb 15; ...