Also known as antihemophilic globulin (AHG) or antihemophilic factor VIII. A protein factor in the blood serum that is instrumental in the “cascade” of chemical reactions (involving 1 7 blood components) that leads to clot formation following a cut or other wound to tissue. Also, a deficiency of AHG is the cause of the classical type of hemophilia sometimes known as hemophilia A.
A naturally occurring protein in the plasma that aids in the coagulation of blood. A congenital deficiency of results in the bleeding disorder known as hemophilia A factor VIII concentrate.
A protein that is a constituent of the coagulation cascade an essential component in the clotting of blood. Those people with the inherited disorder haemophilia have abnormally low amounts of factor VIII and so bleed more when cut. They are treated with a concentrated version of the factor to reduce the tendency to bleed.
A crucial protein engaged in the process of blood clotting, which necessitates the presence of von Willebrand factor (vWF) to maintain its stability and ensure its prolonged existence within the bloodstream.
Factor VIII is a crucial blood protein that plays a significant role in blood clotting. Individuals with haemophilia exhibit lower levels of factor VIII in their blood, leading to a tendency for abnormal bleeding and prolonged bleeding when injured.
Individuals with severe haemophilia necessitate regular treatment with factor VIII concentrates. This treatment effectively minimizes the bleeding tendency and enables the affected person to lead a normal quality of life.