Case Report: Common variable immunodeficiency phenotype and granulomatous–lymphocytic interstitial lung disease with a novel SOCS1 variant

Common variable immunodeficiency is a heterogeneous symptomatic group of inborn errors of immunity that mainly affects antibodies production and/or function, predisposing patients to recurrent and severe infections. More than half of them usually develop autoimmunity, lymphoproliferation, enteropath...

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Autors principals:	María Soledad Caldirola, Espantoso Daiana, Andrea Cecilia Gomez Raccio, Ana Luz García, Agustin Bernacchia, Martín Medín, Maria Isabel Gaillard, Daniela Di Giovanni
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2024-06-01
Col·lecció:	Frontiers in Pediatrics
Matèries:	common variable immunodeficiency granulomatous–lymphocytic interstitial lung disease SOCS1 GLILD inborn errors of immunity
Accés en línia:	https://www.frontiersin.org/articles/10.3389/fped.2024.1423858/full
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