Description of the disease * EnglishPolish Pobierz sekcję do PDF 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 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl