ANCA vasculitis expands the spectrum of autoimmune manifestations of activated PI3 kinase δ syndrome

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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Bibliographic Details
Main Authors: Amika K. Sood, Olivia Francis, Stephen A. Schworer, Steven M. Johnson, Benjamin D. Smith, Paul B. Googe, Eveline Y. Wu
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-05-01
Series:Frontiers in Pediatrics
Subjects:
activated PI3 kinase delta syndrome
autoimmune
ANCA vasculitis
immunodeficiency
inborn errors of immunity
immune dysregulation
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2023.1179788/full

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https://www.frontiersin.org/articles/10.3389/fped.2023.1179788/full

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