Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
Department of Pediatrics, Kagawa University, Kagawa, Japan.
Pediatr Blood Cancer. 2024 Mar;71(3):e30834. doi: 10.1002/pbc.30834. Epub 2023 Dec 27.
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.
Diamond-Blackfan 贫血(DBA)是一种先天性红细胞生成障碍性贫血。大多数致病基因是核糖体蛋白。GATA1 是一种造血主转录因子,也是导致 DBA 的原因。GATA1 位于 Xp11.23;因此,DBA 仅在男性中以 X 连锁遗传模式发生。在这里,我们报告了一例女性新生儿暂时性成红细胞减少症和中度贫血的病例,该患者存在 GATA1 新生变异。在该患者中,红系细胞中观察到 GATA1 野生型等位基因的甲基化增加。GATA1 的偏 Lyon 化可能导致女性患者出现轻度短暂性成红细胞减少症。