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Up to: Coagulation protein disease
Von Willebrand disease (hereditary or acquired)
Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von Willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include bruises, nose bleeding, gum bleeding following a dental procedure, heavy menstrual bleeding, and gastrointestinal bleeding.
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Hereditary von Willebrand disease 18 trials · 29 incl. sub-types Sub-types →
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Acquired von willebrand syndrome 3 trials