Abdul Jalal MJ, Mohammed Iqbal KM, Nusaiba K and Basheer S
Immune Thrombocytopenic Purpura (ITP) is an autoimmune disorder with isolated thrombocytopenia marked by peripheral blood platelet count<100 × 109/L without any other etiology or disorders that may be associated with thrombocytopenia. The treatment of newly diagnosed ITP patients is steroids. However, about one-third of patients do not respond to steroids. Here, we present a 63-yearold hypothyroid, hypertensive, and diabetic female presented with a history of bruising of skin in multiple sites.
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