LOC100506136
Description:
Von Willebrand disease (VWD) is an inherited bleeding disorder characterized by a deficiency or dysfunction of the von Willebrand factor (VWF), a protein that plays a crucial role in blood clotting. VWD affects both men and women and can range in severity from mild to severe.
Types of VWD:
There are three main types of VWD:
- Type 1: The most common type, characterized by a quantitative deficiency of VWF.
- Type 2: A qualitative deficiency of VWF, with abnormal VWF structure or function.
- Type 3: A severe deficiency or complete absence of VWF.
Associated Diseases:
VWD is often associated with other bleeding disorders, including:
- Hemophilia A
- Hemophilia B
- Platelet disorders
Did you Know ?
- VWD is the most common inherited bleeding disorder, affecting approximately 1 in 10,000 people worldwide.
