ITP (Immune Thrombocytopenic Purpura)

Immune Thrombocytopenic Purpura (ITP) is an autoimmune disorder where the immune system mistakenly attacks and destroys platelets, the blood cells responsible for clotting. This results in a low platelet count, increasing the risk of easy bruising, bleeding, and small purple spots called purpura on the skin. ITP can develop suddenly or gradually and may be triggered by infections or other factors. While often manageable, it sometimes requires treatment to boost platelet levels or suppress immune activity. The condition varies in severity and can resolve on its own or become chronic, necessitating ongoing medical care.