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- W4247206594 abstract "Von Willebrand disease (VWD) is the most common inherited bleeding disorder, affecting as much as 1% of the general population, and equally affects both sexes as well as all races and ethnicities. VWD should be suspected in the patient with platelet-type bleeding and a family history of a bleeding diathesis. The clinical features of VWD can be quite variable. Screening tests are of little value in making the diagnosis of VWD. The goal of treatment in VWD is to control or prevent serious or life-threatening bleeding. Acquired von Willebrand syndrome (AVWS) refers to defects in VWF concentration, structure, or function that are not inherited directly but are consequences of other medical disorders. It is usually caused by one of three mechanisms: autoimmune clearance or inhibition of VWF, increased shear-induced proteolysis of VWF, or increased binding of VWF to platelets or other cell surfaces." @default.
- W4247206594 created "2022-05-12" @default.
- W4247206594 date "2021-02-05" @default.
- W4247206594 modified "2023-09-24" @default.
- W4247206594 title "Von Willebrand Disease" @default.
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- W4247206594 doi "https://doi.org/10.1002/9781119210771.ch8" @default.
- W4247206594 hasPublicationYear "2021" @default.
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