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...

Full description

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

Similar Items

Similar Items