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Primary acquired pure red cell aplasia

Disease definition

A rare acquired aplastic anemia characterized by a severe normocytic anemia with normal peripheral leukocyte and platelet counts, reticulocytopenia, high serum ferritin and transferrin saturation levels and isolated, almost complete absence of erythroblasts in the bone marrow with normal granulopoesis and megakaryopoesis. It presents with signs of severe anemia (fatigue, lethargy, pallor, intolerance of physical exercise and exertional dyspnea) in the absence of hemorrhagic symptoms.

ORPHA:98872

Classification level: Disorder
  • Synonym(s):
    • Primary acquired PRCA
  • Prevalence: -
  • Inheritance: -
  • Age of onset: -
  • ICD-10: D60.0
  • ICD-11: 3A61
  • OMIM: -
  • UMLS: C4707560
  • MeSH: -
  • GARD: 10898
  • MedDRA: -

  A summary on this disease is available in Deutsch (2018) Español (2018) Italiano (2018) Nederlands (2018) Polski ()

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

Newborn screening

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