Tag: Type 3 vwd

Affecting about 1 in 500,000 people, a condition defined by what is the absence of VWF, or Type 3 Von Willebrand Disease, is the rarest and most severe form of this inherited bleeding disorder. This critical deficiency has profound effects on the body's ability to form blood clots and stop bleeding.

Over 1% of the global population may be affected by von Willebrand disease (vWD), but the severity varies widely between different types. Understanding the specific form of the disease is crucial for effective management and is the first step toward determining which form of von Willebrand disease is the most severe.