Acquired elliptocytosis as presenting sign of a myelodysplastic syndrome associated with deletion of chromosome 20 and mutations in TET2, DNMT3A, and U2AF1
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00277-020-04368-w.pdf
Reference10 articles.
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2. Rummens JL, Verfaille C, Criel A, Hidajat M, Vanhoof A, Van den Berghe H, Louwagie A (1986) Elliptocytosis and schistocytosis in myelodysplasia: report of two cases. Acta Haematol 75(3):174–177
3. Ideguchi H, Yamada Y, Kondo S, Tamura K, Makino S, Hamasaki N (1993) Abnormal erythrocyte band 4.1 protein in myelodysplastic syndrome with elliptocytosisi. Brit J Haematol 85(2):387–392
4. Ishida F, Shimodaira S, Kobayashi H, Saito H, Kaku M, Kanzaki A, Yawata Y, Kitano K, Kiyosawa K (1999) Elliptocytosis in myelodysplastic syndrome associated with translocation (1;5)(p10;q10) and deletion of 20q. Cancer Genet Cytogenet 108:162–165
5. Hur M, Lee KM, Cho HC, Park YI, Kim SH, Chang YW, Kim YR, Cho HI (2004) Protein 4.1 deficiency and deletion of chromosome 20q are associated with acquired elliptocytosis in myelodysplastic syndrome. Clin Lab Haematol 26:69–72
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1. Acquired elliptocytosis in chronic myeloid neoplasms: An enigmatic relationship to acquired red cell membrane protein and genetic abnormalities;Blood Cells, Molecules, and Diseases;2023-11
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