Idiopathic Thrombocytopenic Purpura

Idiopathic thrombocytopenic purpura (ITP) is an autoimmune disorder in which the body’s immune system mistakenly attacks and destroys platelets, the small blood cells responsible for blood clotting. The decreased platelet count leads to easy bruising, bleeding gums, prolonged bleeding after an injury, or bleeding in the brain. Without proper diagnosis and treatment, ITP can be fatal. Treatment for ITP may include steroids, intravenous antibodies, splenectomy (surgical removal of the spleen), or a combination of these. With treatment, many patients have a full recovery and can lead a normal life.

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Prevalence of Impulse Control Disorders among Adult Filipino Patients with Idiopathic Parkinson’s Disease seen at Jose R. Reyes Memorial Medical Center

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A Bit Exagerrated Role of Complete Blood Count Parameters on the Prognosis of Idiopathic Sudden Sensorineural Hearing Loss

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Juvenile Idiopathic Arthritis: A Study of 74 Cases in Northeast Brazil

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Juvenile Idiopathic Arthritis in a New Rheumatology Clinic in Nigeria

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The Elliptical Aggregates – Idiopathic Granulomatous Mastitis

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Evolution of Janus Kinase 2 V617F-negative idiopathic myelofibrosis into Philadelphia+ chronic myeloid leukemia

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