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Von Willebrand disease type 2B

ORPHA:166087· ICD-10 D68.0

Definition

A subtype of type 2 von Willebrand disease characterized by a bleeding disorder associated with increased affinity of the Willebrand factor (VWF) for platelets leading to rapid clearance of both the platelets (increasing the risk of thrombocytopenia) and VWF from the plasma. The disease manifests as mucocutaneous bleeding (menorrhagia, epistaxis, gastrointestinal hemorrhage, etc.).

Prevalence
Unknown
Inheritance
Autosomal dominant