Immune thrombocytopenic purpura may not cause any symptoms or may have symptoms that are easily confused with other diseases. Therefore, without knowledge about autoimmune thrombocytopenia, the disease will be detected late and the risk of complications is very high.

Immune thrombocytopenic purpura, also known as immune thrombocytopenic purpura, is an immune disease, which is a condition of thrombocytopenia caused by antibodies that can self-generate and adhere to platelet membrane antigens, causing symptoms of thrombocytopenia in peripheral blood. The disease needs to be detected and treated properly to avoid causing some dangerous complications.

Idiopathic thrombocytopenic purpura is an autoimmune disease in humans, caused by a decrease in platelets in the body and affects the body's ability to stop bleeding and clot blood when there is a wound or slight impact. The disease is common in all ages, but the most common is thrombocytopenic purpura in newborns and often leaves very serious complications.

Immune thrombocytopenia (ITP) is a blood clotting disorder. It is caused by a low platelet count because the immune system attacks healthy platelets. If you are not bleeding and your platelet count is not too low, no treatment is needed. However, if your condition becomes more severe, you may need medication or surgery.