C70548Level 7
Acquired Pure Red Cell Aplasia
**Semantic type:** Disease or Syndrome
**Definition:** A disease characterized by normocytic, normochromic anemia, low hematocrit, reticulocytopenia and selective erythroid hypoplasia. It can occur as a chronic or acute form; the former is predominantly seen in adults and the latter in children. Pathogenesis involves immune dysfunction with antibodies directed against erythroid precursor cells or erythropoietin, or due to T-cell mediated suppression of erythropoiesis.
**Synonyms:** - acquired pure red cell aplasia
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