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  1. Platelets are cells that circulate in the bloodstream and help blood clot. The blood usually contains about 140,000 to 440,000 platelets per microliter (140 to 440 × 109 per liter). When the platelet count falls below about 50,000 platelets per microliter of blood (50 × 109 per liter), bleeding can occur even after relatively minor injury.

  2. Symptoms and Signs of Von Willebrand Disease Bleeding manifestations in the most common type I von Willebrand disease (VWD) include bruising, mucosal bleeding, bleeding from small skin cuts that may stop and start over hours, increased menstrual bleeding, and sometimes bleeding after surgical procedures (eg, tooth extraction, tonsillectomy).

  3. These symptoms may include: Heavy menstrual bleeding: excessive or prolonged bleeding during monthly period. This is a critical issue for females which affects up to 95% of women with von Willebrand disease. Metrorrhagia: bleeding between periods. Postpartum bleeding: heavy bleeding or hemorrhage during or after labor and delivery.

  4. 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.

  5. Apr 16, 2024 · von Willebrand disease (VWD) is a bleeding disorder. It can be inherited or, less commonly, it can develop later in life (this type of VWD is not heritable and is referred to as acquired von Willebrand syndrome [AVWS]). The amount of bleeding and need for treatment varies from person to person, with some never needing treatment (or even knowing ...

  6. Feb 25, 2019 · Von Willebrand’s disease is the most common type of heritable bleeding disorder. Type 1 is the most prevalent, affecting around 60–80 percent of all people with the condition.

  7. Nov 29, 2018 · Definition. Von Willebrand disease (VWD), the most common inherited bleeding disorder, is due to either a quantitative or qualitative abnormality of von Willebrand factor (VWF). VWF provides the critical link between platelets and exposed vascular subendothelium, and also binds and stabilises coagulation factor VIII.

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