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"Afibrinogenemia," congenital
- ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov AFIBRINOGENEMIA, CONGENITAL PubMed Casini A, Lukowski S, Quintard VL, Crutu ...
- ... Mutations in the FGA gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... to the excessive bleeding seen in people with congenital afibrinogenemia. More About This Health Condition Mutations in one ...
- ... Mutations in the FGB gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion. Blood. 2000 Feb 15; ...
- ... Mutations in the FGG gene can lead to congenital afibrinogenemia, a condition that causes excessive bleeding due to ... to the excessive bleeding seen in people with congenital afibrinogenemia. More About This Health Condition Mutations in one ...
- Rare Clotting Factor Deficiencies (World Federation of Hemophilia)Bleeding Disorders/Specifics ... Bleeding Disorders ... Vitamin K/Learn More ... Vitamin K ... World Federation of Hemophilia
- Congenital fibrinogen deficiency is a very rare, inherited blood disorder in which the blood does not clot normally. It affects a protein called fibrinogen. This protein is needed for the blood to clot.