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Case Reports
. 2021 Oct;41(7):1683-1685.
doi: 10.1007/s10875-021-01092-6. Epub 2021 Jul 12.

Myelodysplastic Syndrome in a Patient with IPEX Syndrome

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Case Reports

Myelodysplastic Syndrome in a Patient with IPEX Syndrome

Daisuke Toyama et al. J Clin Immunol. 2021 Oct.
No abstract available

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References

    1. Gambineri E, Perroni L, Passerini L, et al. Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity. J Allergy Clin Immunol. 2008;122:1105-12.e1. - DOI
    1. Hoshino A, Kanegane H, Nishi M, et al. Identification of autoantibodies using human proteome microarrays in patients with IPEX syndrome. Clin Immunol. 2019;203:9–13. - DOI
    1. McMurchy AN, Gillies J, Allan SE, et al. Point mutants of forkhead box P3 that cause immune dysregulation, polyendocrinopathy, enteropathy, X-linked have diverse abilities to reprogram T cells into regulatory T cells. J Allergy Clin Immunol. 2010;126:1242–51. - DOI
    1. Yamauchi T, Takasawa K, Kamiya T, et al. Hematopoietic stem cell transplantation recovers insulin deficiency in type 1 diabetes mellitus associated with IPEX syndrome. Pediatr Diabetes. 2019;20:1035–40. - DOI
    1. Seidel MG. Autoimmune and other cytopenias in primary immunodeficiencies: pathomechanisms, novel differential diagnoses, and treatment. Blood. 2014;124:2337–44. - DOI

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