Catalog

Von Willebrand disease

3B12

Link to WHO Definition

Von Willebrand disease – http://id.who.int/icd/entity/2112021600

A disease caused by inherited genetic mutations. This disease is characterised by quantitative, structural or function abnormalities of von Willebrand factor leading to abnormalities in coagulation of the blood. This disease may present with prolonged bleeding, easy bruising or bleeding gums. Confirmation is by identification of mutation through genetic testing.

Parents

Children