Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency

Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive disease associated with a highly variable clinical presentation, including vasculitis, immunodeficiency, and hematologic manifestations, potentially progressing over time. The present study describes the long-term evolution of the...

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Detalles Bibliográficos
Autores principales: Barzaghi, Federica, Cicalese, Maria Pia, Zoccolillo, Matteo, Brigida, Immacolata, Barcella, Matteo, Merelli, Ivan, Sartirana, Claudia, Zanussi, Monica, Calbi, Valeria, Bernardo, Maria Ester, Tucci, Francesca, Migliavacca, Maddalena, Giglio, Fabio, Doglio, Matteo, Canarutto, Daniele, Ferrua, Francesca, Consiglieri, Giulia, Prunotto, Giulia, Saettini, Francesco, Bonanomi, Sonia, Rovere-Querini, Patrizia, Di Colo, Giulia, Jofra, Tatiana, Fousteri, Georgia, Penco, Federica, Gattorno, Marco, Hershfield, Michael S., Bongiovanni, Lucia, Ponzoni, Maurilio, Marktel, Sarah, Milani, Raffaella, Peccatori, Jacopo, Ciceri, Fabio, Mortellaro, Alessandra, Aiuti, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557171/
https://www.ncbi.nlm.nih.gov/pubmed/36248833
http://dx.doi.org/10.3389/fimmu.2022.910021

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557171/
https://www.ncbi.nlm.nih.gov/pubmed/36248833
http://dx.doi.org/10.3389/fimmu.2022.910021

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