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ITP Disease: Symptoms and Treatments Idiopathic Thrombocytopenic Purpura ( ITP ), also known as immune thrombocytopenia, is an autoimmune disorder. Characterized by a low platelet count, ITP can lead to excessive bleeding and bruising. In this condition, the immune system mistakenly attacks and destroys platelets, which are essential for normal blood clotting. As a result, individuals with ITP may experience prolonged bleeding and excessive bruising. Autoimmune Thrombocytopenic Purpura: Signs, Causes, and How to Treat Autoimmune Thrombocytopenic Purpura, also known as ITP , is a condition where the immune system mistakenly attacks and destroys platelets, which are cells that help blood to clot. This can lead to a low platelet count and an increased risk of bleeding. The exact cause of ITP is not fully understood, but it is believed to involve a malfunction in the immune system where it mistakenly targets platelets as foreign invaders ... We would like to show you a description here but the site won’t allow us. In short, ITP is an illness in which unusually low levels of platelets lead to purpura and other forms of abnormal bleeding. In people with ITP , the immune system produces abnormal proteins called antiplatelet antibodies.
