Bleeding disorders encompass a group of conditions characterized by impaired blood clotting, leading to prolonged or spontaneous bleeding. These disorders can affect both children and adults, posing significant health challenges. Hemophilia, a well-known hereditary bleeding disorder, results from deficient or dysfunctional clotting factors. Von Willebrand disease, another common disorder, involves a deficiency in a specific clotting protein. Inherited and acquired factors contribute to bleeding disorders, affecting various aspects of the coagulation cascade. Timely diagnosis is crucial, involving blood tests and clinical assessments. Treatment often includes clotting factor replacement, medications, and lifestyle adjustments. Managing bleeding disorders requires a multidisciplinary approach, integrating medical intervention and patient education.