What is congenital afibrinogenemia?

Congenital afibrinogenemia is an inherited (genetic) blood disorder in which the blood doesn't clot normally because there is a lack of blood clotting factor I. Therefore patients are at a higher risk for bleeding. Symptoms include bruising, and excessive bleeding after surgery or injury.

How do members experience congenital afibrinogenemia?

*Reports may be affected by other conditions and/or medication side effects. We ask about general symptoms (anxious mood, depressed mood, fatigue, pain, and stress) regardless of condition.