Protein C Deficiency Disease
Protein C deficiency is a rare but significant hereditary or acquired disorder of the coagulation system, characterized by an increased risk of thromboembolic events due…
Hypoprothrombinemia: Causes, Symptoms, and Treatment
Hypoprothrombinemia is a rare blood disorder characterized by a deficiency in prothrombin (Factor II), a protein essential for blood clotting. This condition can lead to…
Hypofibrinogenemia: Causes, Symptoms
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…
Hereditary Factor X Deficiency Disease
Hereditary Factor X Deficiency Disease is a rare genetic disorder characterized by impaired blood clotting due to insufficient or malfunctioning Factor X protein. This condition…
Hemophilia B: Causes, Symptoms, Diagnosis, and Treatment
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: Causes, Symptoms, and Treatment
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…
Disseminated intravascular coagulation
Disseminated Intravascular Coagulation (DIC) is a serious medical condition characterized by widespread activation of the clotting cascade, leading to both clot formation and bleeding. This…