Immune thrombocytopenia (ITP) is an autoimmune disease characterized by a low platelet count caused by accelerated platelet destruction and/or impaired platelet production. Chronic ITP is defined as ITP lasting for… Click to show full abstract
Immune thrombocytopenia (ITP) is an autoimmune disease characterized by a low platelet count caused by accelerated platelet destruction and/or impaired platelet production. Chronic ITP is defined as ITP lasting for more than 12 months.[1][1] T-cell abnormalities are implicated in ITP pathogenesis.
               
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