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Article Synopsis
  • A nationwide study involving 2402 patients investigated the prevalence of glycosylphosphatidylinositol-anchored protein-deficient (GPI[-]) cells, specifically PNH-type cells, in individuals with acquired aplastic anaemia (AA) and myelodysplastic syndrome (MDS) using high-sensitivity flow cytometry.
  • PNH-type cells were found in 52.6% of AA patients and 13.7% of MDS patients, while none were present in patients with refractory anaemia having ringed sideroblasts or excess blasts.
  • The study concluded that PNH-type granulocyte levels can change over time in patients with AA and highlighted that having ≥1% PNH-type granul
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