Congenital Afibrinogenemia

Congenital Afibrinogenemia is a rare bleeding disorder that occurs due to the absence of fibrinogen, a protein that helps in blood clotting. It is an inherited condition that is present at birth and affects both males and females equally. Individuals with Congenital Afibrinogenemia are at a higher risk of bleeding episodes, including spontaneous bleeding, excessive bleeding after injury or surgery, and bleeding into the joints and muscles.