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  1. Mar 31, 2023 · Von Willebrand disease (vWD) is a common, inherited, genetically and clinically heterogeneous hemorrhagic disorder caused by a deficiency or dysfunction of the protein termed von Willebrand...

  2. Jan 20, 2022 · von Willebrand disease is the most common inherited bleeding abnormality, with a prevalence rate of 0.8-1.3%. This disorder is secondary to a decrease or defect in the von Willebrand portion...

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  4. What causes inherited von Willebrand factor deficiency? What causes acquired von Willebrand factor deficiency? How are specimens collected for a von Willebrand factor ristocetin...

  5. The course and outcome of pregnancy in women with different types of von Willebrand disease (3 type I, 1 subtype IIA, and 1 subtype IIB) are described. In all patients, factor VIII increased...

  6. OBJECTIVE: To assess the obstetric outcome in women with von Willebrand's disease or factor XI deficiency. SETTING: Haemophilia Centre and Haemostasis Unit, The Royal Free Hospital.

  7. Jun 21, 2011 · If you know that a patient has the serious bleeding disorder known as von Willebrand disease, find out how to test and treat in this update from the CDC.

  8. Nov 20, 2020 · Among congenital bleeding disorders involving platelets, type III von Willebrand disease and type I Glanzmann thrombasthenia are severe diseases associated with lifelong hemorrhages. Most other...

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