Von Willebrand factor (vWF) is a blood glycoprotein involved in hemostasis.
the body does not produce enough of a protein called von Willebrand factor(vWF) or produces abnormal vWF
Von Willebrand's disease can be treated with desmopressin (DDAVP, Stimate).
The von Willebrand disease creates the tendency to bleed and bruise easily. It is an inherited clotting disorder that is usually less severe but more common. Those affected lack a plasma protein. Von Willebrand factor enables platelets to adhere to damaged blood vessel walls.
von Willebrand disease results from inadequate von Willebrand factor. This problem is a blood clotting disorder.
Von Willebrand disease may be hard to diagnose. Low Von Willebrand factor levels and bleeding do not always mean you have Von Willebrand disease. http://www.nlm.nih.gov/medlineplus/ency/article/000544.htm
The Finnish physician Erik von Willebrand was the first to describe von Willebrand disease (VWD).
Th Vukovich has written: 'The influence of human factor VIII/von Willebrand factor on human blood platelet aggregation' -- subject(s): Von Willebrand disease, Blood platelets, Aggregation
A protein found in the blood that is involved in the process of blood clotting.
The von Willebrand disease creates the tendency to bleed and bruise easily. It is an inherited clotting disorder that is usually less severe but more common. Those affected lack a plasma protein. Von Willebrand factor enables platelets to adhere to damaged blood vessel walls.
Unfortunately you will not be able to grow out of von Willebrand's.
Von Willebrand's syndrome is a deficiency in the blood coagulation cascade. Specifically coag. factor 8. Coag factor 8 comes in 2 parts, von willebrand protein and another smaller glycoprotein. Heavy drinking may manifest some similar symptoms, but it's doubtful that it can be attributed to hemophilia related disease.