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Von Willebrand disease (VWD) is a hereditary deficiency of von Willebrand factor (VWF), which causes platelet dysfunction. Bleeding tendency is usually mild. Von Willebrand disease (VWD) is a genetic bleeding disorder that is passed down from parent to child and affects both men and women. von Willebrand Disease (abbreviated vWD) is an inherited bleeding disorder caused by lack of von Willebrand factor protein (vWF). This protein circulates in.

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Von Willebrand disease is the most common inherited bleeding disorder among American women, with a prevalence of –% 1. The overall prevalence is even. Von Willebrand Disease is caused by low amounts or structural abnormalities in a protein called Von Willebrand Factor. This results in prolonged clotting. Von Willebrand disease (VWD) is an inherited disorder that affects the blood's ability to clot. People with VWD may experience heavy bleeding after an.

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Von Willebrand disease (VWD) is a blood disorder in which the blood does not clot properly. It is a chronic disease that affects the circulatory system. Von Willebrand disease is typically an inherited disease caused by variations (mutations) in the VWF gene. The VWF gene provides instructions for making a. Von Willebrand disease, a bleeding disorder that slows down the blood clotting process, affects up to 1% of people in the United States.