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Chronic immune thrombocytopenic purpura (cITP)cITP is an acquired autoimmune disorder that causes excessive bruising and bleeding resulting from unusually low levels of platelets. cITP is among the most common bleeding disorders and is nearly three times more prevalent than hemophilia. cITP is associated with significant morbidity and mortality and is often highly problematic for patients—complicating employability, insurability, and overall quality of life (QoL). Children may develop cITP after a viral infection and usually recover fully without treatment. In adults, however, the disorder is often long-term.1,2Materials

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References:
  1. Ansteatt KT, Unzicker CJ, Hurn ML, et al. The need for comprehensive care for persons with chronic immune thrombocytopenic purpura. J Blood Med. 2020;11:457-463. doi: 10.2147/JBM.S289390. Accessed June 16, 2022. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7751596/
  2. Immune thrombocytopenia (ITP). Mayo Clinic. Accessed June 16, 2022. https://www.mayoclinic.org/diseases-conditions/idiopathic-thrombocytopenic-purpura/symptoms-causes/syc-20352325

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