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Transient erythroblastopenia due to a GATA1 variant in an infant female.

Motoi YamashitaTakahiro TomodaAmi MizuoTakeshi IsodaMakiko EgawaMasayuki YoshidaTsutomu TokiKo KudoKiminori TeruiEtsuro ItoTomohiro MorioMasatoshi Takagi
Published in: Pediatric blood & cancer (2023)
Diamond-Blackfan anemia (DBA) is a congenital anemia with erythroid cell aplasia. Most of the causative genes are ribosomal proteins. GATA1, a hematopoietic master transcription factor required for erythropoiesis, also causes DBA. GATA1 is located on Xp11.23; therefore, DBA develops only in males in an X-linked inheritance pattern. Here, we report a case of transient erythroblastopenia and moderate anemia in a female newborn infant with a de novo GATA1 variant. In this patient, increased methylation of the GATA1 wild-type allele was observed in erythroid cells. Skewed lyonization of GATA1 may cause mild transient erythroblastopenia in a female patient.
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