
von Willebrand disease - Wikipedia
Von Willebrand disease (VWD) is the most common hereditary blood-clotting disorder in humans. An acquired form can sometimes result from other medical conditions. [1] It arises from a deficiency in the quality or quantity of von Willebrand factor (VWF), a multimeric protein that is required for platelet adhesion.
About von Willebrand Disease | Von Willebrand Disease (VWD)
2024年5月15日 · Von Willebrand disease (VWD) is a blood disorder in which the blood does not clot properly. VWD is the most common bleeding disorder. Signs of VWD include nosebleeds, easy bruising, heavy menstrual bleeding, and longer than normal bleeding after injury, surgery, dental work, or childbirth.
Vicenza VWD was first described as a variant of VWD in which the level of plasma VWF is usually <15 IU/dL and the VWF multimers are even larger than normal, like the ultralarge multimers characteristic of platelet VWF.92 The low level of VWF in plasma in Vicenza VWD appears to be explained by the effect of a specific mutation, Arg1205His, that ...
Von Willebrand Disease (VWD) - University of Rochester Medical Center
Von Willebrand disease (VWD) is an inherited disorder that affects the blood's ability to clot. What causes VWD? VWD is almost always inherited. This means it is passed from parents to children. People with the disorder may have low levels of a blood protein called von Willebrand factor.
Von Willebrand Disease – Symptoms and Causes | Penn Medicine
Named after the doctor who discovered it, von Willebrand disease (VWD) is an inherited bleeding disorder that impacts the body’s ability to make blood clots. VWD is the most common inherited bleeding disorder. Formation of blood clots depends on a process where proteins called clotting factors join platelets, a type of blood cell.
Patient education: von Willebrand disease (Beyond the Basics)
2025年1月22日 · There are three major types of inherited von Willebrand disease (VWD), named 1, 2, and 3: Type 1 is the most common form, affecting approximately three-quarters of people who have inherited VWD.
von Willebrand Disease - University of Utah Health
Von Willebrand disease (VWD) is a genetic bleeding disorder that is passed down from parent to child and affects both men and women. People with VWD do not make enough protein — known as the von Willebrand factor (VWF). This protein is needed for platelets in the blood to form clots and stop or prevent bleeding.
1 VWD is the most common form. People with type 1 VWD have lower than normal levels of VWF, ranging from sligh ly reduced, to very low levels. There is a subtype, type 1C, where VWF does not last as long in the body (meaning
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