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ANCA vasculitis expands the spectrum of autoimmune manifestations of activated PI3 kinase δ syndrome
Activated phosphoinositide 3-kinase δ syndrome (APDS) is a combined immunodeficiency with a broad clinical phenotype, including not only an increased propensity for sinopulmonary and herpesviruses infections but also immune dysregulation, such as benign lymphoproliferation, autoimmunity, and maligna...
Autores principales: | Sood, Amika K., Francis, Olivia, Schworer, Stephen A., Johnson, Steven M., Smith, Benjamin D., Googe, Paul B., Wu, Eveline Y. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235767/ https://www.ncbi.nlm.nih.gov/pubmed/37274825 http://dx.doi.org/10.3389/fped.2023.1179788 |
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