Cargando…
Natural history of type 1 diabetes on an immunodysregulatory background with genetic alteration in B-cell activating factor receptor: A case report
The immunological events leading to type 1 diabetes (T1D) are complex and heterogeneous, underscoring the necessity to study rare cases to improve our understanding. Here, we report the case of a 16-year-old patient who showed glycosuria during a regular checkup. Upon further evaluation, stage 2 T1D...
Autores principales: | Di Lorenzo, Biagio, Pacillo, Lucia, Milardi, Giulia, Jofra, Tatiana, Di Cesare, Silvia, Gerosa, Jolanda, Marzinotto, Ilaria, Zapparoli, Ettore, Rivalta, Beatrice, Cifaldi, Cristina, Barzaghi, Federica, Giancotta, Carmela, Zangari, Paola, Rapini, Novella, Deodati, Annalisa, Amodio, Giada, Passerini, Laura, Carrera, Paola, Gregori, Silvia, Palma, Paolo, Finocchi, Andrea, Lampasona, Vito, Cicalese, Maria Pia, Schiaffini, Riccardo, Di Matteo, Gigliola, Merelli, Ivan, Barcella, Matteo, Aiuti, Alessandro, Piemonti, Lorenzo, Cancrini, Caterina, Fousteri, Georgia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459137/ https://www.ncbi.nlm.nih.gov/pubmed/36090979 http://dx.doi.org/10.3389/fimmu.2022.952715 |
Ejemplares similares
-
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients
por: Cifaldi, Cristina, et al.
Publicado: (2021) -
Case Report: EBV Chronic Infection and Lymphoproliferation in Four APDS Patients: The Challenge of Proper Characterization, Therapy, and Follow-Up
por: Rivalta, Beatrice, et al.
Publicado: (2021) -
Phenotypical T Cell Differentiation Analysis: A Diagnostic and Predictive Tool in the Study of Primary Immunodeficiencies
por: Attardi, Enrico, et al.
Publicado: (2019) -
Targeted treatment of autoimmune cytopenias in primary immunodeficiencies
por: Pacillo, Lucia, et al.
Publicado: (2022) -
Urogenital Abnormalities in Adenosine Deaminase Deficiency
por: Pajno, Roberta, et al.
Publicado: (2020)