Congenital dyserythropoietic anemia type IV with kruppel-like factor 1 E325K mutation in a preterm neonate: Case and literature review
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Reference12 articles.
1. A very rare congenital dyserythropoietic anemia variant-type IV in a patient with a novel mutation in the KLF1 gene: A case report and review of the literature;Belgemen-Ozer;J Pediatr Hematol Oncol,2020
2. Congenital dyserythropoietic anemias;Iolascon;Blood,2020
3. Congenital dyserythropoietic anaemia with novel intra-erythroblastic and intra-erythrocytic inclusions;Wickramasinghe;Br J Haematol,1991
4. A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia;Arnaud;Am J Hum Genet,2010
5. Jaffray JA, Mitchell WB, Gnanapragasam MN, et al. Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: Review of all reported cases and development of a clinical diagnostic paradigm. Blood Cells Mol Dis 2013;51:71-5.
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1. Congenital dyserythropoietic anemia type IV with KLF1 E325K mutation: A new case with dysmorphic male genitalia;Pediatric Blood & Cancer;2024-03-24
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