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Acquired von Willebrand syndrome

ORPHA:99147· ICD-10 D68.4

Definition

A rare bleeding disorder characterized by defects in von Willebrand factor, similar to those seen in hereditary von Willebrand disease (VWD), but which are caused by an underlying pathology, generally in elderly patients without any personal or family history of bleeding anomalies.

Prevalence
<1 / 1 000 000
Inheritance
Not applicable
Age of onset
Adult