Transient erythroblastopenia of childhood

Orpha code: 98871OMIM code: 227050

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.

Disease data
Classification

Disease

Synonyms
Transient acquired pure red cell aplasia
Przejściowa nabyta aplazja czysto czerwonokrwinkowa
ORPHA code
98871
OMIM code
227050
ICD10 code
D60.1
ICD11 code
3A61.0

No additional description.

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