ENFERMEDAD DE DIGEORGE

REFERENCIAS BIBLIOGRÁFICAS
·Collins, C., Sharpe, E., Silber, A., Kulke, S., & Hsieh, E. W. Y. (2021). Congenital Athymia: Genetic Etiologies, Clinical Manifestations, Diagnosis, and Treatment. Journal of Clinical Immunology, 41(5), 881–895.
·Mahdaviani, A., et al. (2023). Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development. Journal of Clinical Immunology, 43(2), 247–270.
·Systematic Review Authors. (2024). Thymus transplantation for DiGeorge Syndrome: a systematic review. [Revista], (hasta septiembre 2024). (Se incluyeron 16 estudios). (PubMed)
·Mende, C., et al. (2023). A model for preservation of thymocyte-depleted thymus. Brazilian Journal of Medical and Biological Research, 56, e12647.
·Science Publishing Group. (2025). De novo Thymus Reconstitution: The Rising of Cell-based Strategies. International Journal of Immunology, 13(1), 9–22. (Science Publishing Group)
·Süleyman, M., Cagdas, D., Kiper, P. Ö. Ş., et al. (2025). Clinical and Immunological Features of a Large DiGeorge Syndrome Cohort. Journal of Clinical Immunology, 45, 103. (SpringerLink)
·de Wallau, M. B., Xavier, A. C., Moreno, C. A., Kim, C. A., Mendes, E. L., Ribeiro, E. M., … Vieira, T. P. (2024). 22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity. Genes, 15(4), 518. (MDPI)
·NORD. (2024, noviembre 10). Congenital Athymia. En Rare Diseases Database. (National Organization for Rare Disorders)


314-A ARAGÓN FIGUEROA DULCE ESTRELLA