Immune thrombocytopenia (ITP) is a bleeding disorder that keeps your blood from clotting. ITP can be chronic, meaning treatment eases symptoms but doesn’t cure it., Immune thrombocytopenic purpura (ITP), also known as idiopathic thrombocytopenic purpura or immune thrombocytopenia, is an autoimmune primary disorder of hemostasis characterized by a low platelet count in the absence of other causes. [1][2] ITP often results in an increased risk of bleeding from mucosal surfaces (such as the nose or gums) or , Immune thrombocytopenia (ITP) is a platelet disorder caused by problems with your immune system. Learn about the symptoms, causes, and treatments for ITP., Immune thrombocytopenia (ITP), formerly idiopathic thrombocytopenic purpura, is a condition arising from immunoglobulin G (IgG) autoantibodies sensitizing circulating platelets, manifesting as a low platelet count, purpura, and hemorrhagic episodes., Immune thrombocytopenic purpura (ITP) is a bleeding disorder in which the immune system destroys platelets, which are necessary for normal blood clotting. People with the disease have too few platelets in the blood. ITP occurs when certain immune system cells produce antibodies against platelets., Idiopathic Thrombocytopenic Purpura (ITP) is a blood disorder characterized by an abnormal decrease in the number of platelets in the blood. Platelets are cells in the blood that help stop bleeding..