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...

Descripción completa

Detalles Bibliográficos

Autores principales:	María Soledad Caldirola, Espantoso Daiana, Andrea Cecilia Gomez Raccio, Ana Luz García, Agustin Bernacchia, Martín Medín, Maria Isabel Gaillard, Daniela Di Giovanni
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	Frontiers Media S.A. 2024-06-01
Colección:	Frontiers in Pediatrics
Materias:	common variable immunodeficiency granulomatous–lymphocytic interstitial lung disease SOCS1 GLILD inborn errors of immunity
Acceso en línea:	https://www.frontiersin.org/articles/10.3389/fped.2024.1423858/full
Etiquetas:	Agregar Etiqueta Sin Etiquetas, Sea el primero en etiquetar este registro!