Research Notes on Congenital Afibrinogenemia
Congenital afibrinogenemia is a rare, blood disorder wherein there is inability to make fibrinogen that is essential for coagulation. Symptoms may include bruising, nose and gastrointestinal bleeding. Treatment includes transfusion of the blood plasma or blood product containing fibrinogen.
Top Resources on Congenital Afibrinogenemia
- A.D.A.M. (MedlinePlus): Congenital Afibrinogenemia
- Wikipedia: Congenital Afibrinogenemia
- WrongDiagnosis: Introduction: Congenital Afibrinogenemia
- eMedicine: Inherited Abnormalities Of Fibrinogen
- PubMed: Congenital Afibrinogenemia
- Annals of Saudi Medicine: Congenital Afibrinogenemia
- Healthwise (via CIGNA): Afibrinogenemia, Congenital
- TheFreeDictionary: Congenital Afibrinogenemia
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About this WisdomCard
- Contributor: Madeleine Paladar
- Reviewer: Elisa Carter
- Supervised by: The OrganizedWisdom Physician Review Team
- Last update: Jul. 30, 2008
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