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Immune thrombocytopenia (ITP) - Symptoms and causes Immune thrombocytopenia usually happens when the immune system makes a mistake It attacks and destroys the cells that help blood clot, also known as platelets In adults, an infection with HIV, hepatitis or the bacteria that causes stomach ulcers, known as H pylori, can cause ITP
Idiopathic Thrombocytopenic Purpura - Johns Hopkins Medicine Immune thrombocytopenic purpura (ITP) is a blood disorder characterized by a decrease in the number of platelets in the blood Platelets are cells in the blood that help stop bleeding A decrease in platelets can cause easy bruising, bleeding gums, and internal bleeding
ITP in Adults | PDSA In adults, most cases of ITP are either persistent (lasting six to 12 months) or chronic (lasting more than a year) Fortunately, today’s treatments are able to increase your platelet count and restore your overall health
Immune thrombocytopenia (ITP) in adults: Clinical . . . - UpToDate Immune thrombocytopenia (ITP, also called idiopathic thrombocytopenic purpura, immune thrombocytopenic purpura) is an acquired thrombocytopenia caused by autoantibodies against platelet antigens It is one of the more common causes of thrombocytopenia in otherwise asymptomatic adults
Home | US Understanding ITP ITP is a condition where the body's immune system attacks and destroys platelets, which are important for blood clotting This can lead to bleeding, bruising, and other symptoms like fatigue and brain fog, which may be associated with systemic inflammation
ITP — HaemBase My notes are based mostly on the BSH and ASH clinical guidelines The International Working Group (IWG) on ITP also published guidelines in 2019 - they are exhaustive in reviewing the evidence, and can be found here
Understanding ITP Explore multiple dimensions of immune thrombocytopenia (ITP), including what it is, range of symptoms, burden on patients, and ongoing research For US HCPs