Immune thrombocytopenia purpura (ITP) is an autoimmune disease that affects the blood platelets. There is low platelet count even when there is normal bone marrow function. There is also a characteristic purpuric rash which has the tendency to bleed. Symptoms could include bruises, petechiae along the extremities, bleeding from the nose and gums, increased menstrual bleeding and a platelet count below 20,000 per micro liter.
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