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Transient erythroblastopenia of childhood

Disease definition

A rare, benign, red cell aplasia of young children or infants characterized by a normocytic normochromic anaemia with severe reticulocytopenia in otherwise normocellular bone marrow, and a complete spontaneous recovery within 1-2 months after diagnosis. Neutropenia and thrombocytosis may be associated findings at diagnosis, and a history of a preceding viral illness is frequent. No organomegaly is observed.

ORPHA:98871

Classification level: Disorder
  • Synonym(s):
    • Transient acquired pure red cell aplasia
  • Prevalence: -
  • Inheritance: -
  • Age of onset: Infancy, Childhood
  • ICD-10: D60.1
  • ICD-11: 3A61.0
  • OMIM: 227050
  • UMLS: C0238478
  • MeSH: C536980
  • GARD: 7793
  • MedDRA: -

  A summary on this disease is available in Deutsch (2019) Español (2019) Français (2019) Italiano (2019) Nederlands (2019)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.