Creativebiolabs26 Dec, 2023Health
ITP is a kind of thrombocytopenic purpura disease that is defined because of the isolated low platelet count (thrombocytopenia). The patients have normal bone marrow but lack the platelet count. It leads to a characteristic purpuric rash and an increased tendency to bleed. The clinical syndromes are distinct and manifest due to an acute or a chronic condition, respectively. The acute form often induces an infection and has a spontaneous resolution within two months. Chronic immune thrombocytopenia persists longer than six months and the specific cause is also unknown.
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