Introduction Von Willebrand Disease (VWD) is a genetic bleeding disorder characterized by deficiencies or abnormalities in von Willebrand factor (VWF), a protein crucial for normal blood clotting. It affects both males and females and is considered the most common inherited bleeding disorder, impacting approximately 1% of the global population. Understanding its types, causes, symptoms, diagnosis, and treatment options is essential for managing this lifelong condition effectively.   What is Von Willebrand’s Disease? Von Willebrand Disease is named after Erik von Willebrand, a Finnish physician who first described it in the early 20th century. It involves defects in von Willebrand factor,…