Von Willebrand’s disease (vWD) is the most common inherited bleeding disorder, caused by a deficiency or dysfunction of von Willebrand factor (vWF), a crucial protein…
Vitamin K deficiency-induced hypoprothrombinemia is a coagulopathy resulting from impaired synthesis of vitamin K-dependent clotting factors—primarily prothrombin (Factor II). This disorder is characterized by a…
Idiopathic Thrombocytopenic Purpura (ITP) is an autoimmune disorder characterized by an abnormally low platelet count, leading to excessive bruising, bleeding, and other complications. This condition…
Hypofibrinogenemia is a rare blood disorder characterized by abnormally low levels of fibrinogen, a critical protein involved in blood clotting. This condition can lead to…
Hemophilia B, also known as Christmas disease, is a rare inherited bleeding disorder caused by a deficiency of clotting factor IX. This condition leads to…
Hemophilia A is a genetic bleeding disorder caused by insufficient or defective clotting factor VIII. It is the most common type of hemophilia, affecting primarily…