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Congenital fibrinogen deficiency
- Congenital fibrinogen deficiency is a very rare, inherited blood disorder in which the blood does not clot normally. It ...
- ... P, Neerman-Arbez M. FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations. ...
- Bleeding Disorders (National Library of Medicine)Normally, if you get hurt, your body forms a blood clot to stop the bleeding. For blood to clot, your body needs cells called platelets and proteins known as clotting ...
- ... 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
- Blood Clots (National Library of Medicine)What is a blood clot? A blood clot is a mass of blood that forms when platelets, proteins, and cells in the blood stick together. When you get hurt, your ...
- ... Testing Registry: Factor XIII, A subunit, deficiency of Congenital factor XIII deficiency National Organization for Rare Disorders ( ... R, Ariens RA, Muszbek L; Factor XIII And Fibrinogen SSC Subcommittee Of The ISTH. ... of factor XIII deficiencies. J Thromb Haemost. 2011 Jul;9(7):1404- ...
- ... J. Clinical manifestations, management, and molecular genetics in congenital factor VII deficiency: the International Registry on Congenital Factor VII Deficiency (IRF7). Blood. 2000 Jul 1; ...