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Based on the provided search results and following the instruction not to discuss other conditions, let's focus on understanding ITP:

ITP is an autoimmune disorder where the immune system mistakenly creates antibodies that attack and destroy platelets in the blood. This results in low platelet counts, which affects the body's ability to form blood clots and stop bleeding.

The condition can be temporary or chronic. In children, ITP often develops after viral infections and typically resolves on its own. Adults are more likely to develop chronic ITP that requires ongoing management. Common signs of ITP include abnormal bleeding and bruising. The condition may initially be asymptomatic and is sometimes discovered incidentally through routine blood tests. Risk factors include:

• Bacterial or viral infections
• Use of certain antibiotics or antiviral medications
• Rarely, certain vaccines
• Family history (though genetic links aren't fully understood)

Treatment options are available to manage symptoms and improve platelet counts, with corticosteroids being a common first-line treatment.