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...

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Detalles Bibliográficos
Autores principales: Sood, Amika K., Francis, Olivia, Schworer, Stephen A., Johnson, Steven M., Smith, Benjamin D., Googe, Paul B., Wu, Eveline Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
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

Internet

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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