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Congenital dyserythropoietic anemia type I mimicking myelodysplasia syndrome with a novel CDAN1 mutation

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References

  1. Iolascon A, Heimpel H, Wahlin A, Tamary H (2013) Congenital dyserythropoietic anemias: molecular insights and diagnostic approach. Blood 122:2162–2166. https://doi.org/10.1182/blood-2013-05-468223

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H (2002) Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1. Am J Hum Genet 71:1467–1474. https://doi.org/10.1086/344781

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Goasguen JE, Bennett JM, Bain BJ, Brunning R, Vallespi MT, Tomonaga M, Zini G, Renault A, (The International Working Group on Morphology of MDS) (2018) Dyserythropoiesis in the diagnosis of the myelodysplastic syndromes and other myeloid neoplasms: problem areas. Br J Haematol 182:526–533. https://doi.org/10.1111/bjh.15435

    Article  PubMed  Google Scholar 

  4. Locatelli F, Strahm B (2018) How I treat myelodysplastic syndromes of childhood. Blood 131:1406–1414. https://doi.org/10.1182/blood-2017-09-765214

    Article  CAS  PubMed  Google Scholar 

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Funding

This work is supported by the National Natural Science Foundation of China (No. 31701207) to HC and Health Commission of Hubei Province (No. WJ2019M020) to DS.

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Authors and Affiliations

  1. Department of Pediatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

    Xueyan Lv, Fengli Lan, Bingyu Zhang, Hongbo Chen & Runming Jin

  2. Department of Pediatrics, Wuhan Fourth Hospital, Wuhan, China

    Shanwu Dong

  3. Department of Pediatrics, Puai Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

    Shanwu Dong

Authors
  1. Xueyan Lv
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  2. Shanwu Dong
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  3. Fengli Lan
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  4. Bingyu Zhang
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  5. Hongbo Chen
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  6. Runming Jin
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Contributions

FL and BZ collected the data. XL and SD drafted the manuscript. HC and RJ reviewed and finalized the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Hongbo Chen.

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The authors declare that they have no conflict of interest.

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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

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Informed consent was obtained from all individual participants included in the study.

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Lv, X., Dong, S., Lan, F. et al. Congenital dyserythropoietic anemia type I mimicking myelodysplasia syndrome with a novel CDAN1 mutation. Ann Hematol 99, 197–199 (2020). https://doi.org/10.1007/s00277-019-03848-y

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  • DOI: https://doi.org/10.1007/s00277-019-03848-y

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