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...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής

Κύριοι συγγραφείς:	María Soledad Caldirola, Espantoso Daiana, Andrea Cecilia Gomez Raccio, Ana Luz García, Agustin Bernacchia, Martín Medín, Maria Isabel Gaillard, Daniela Di Giovanni
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	Frontiers Media S.A. 2024-06-01
Σειρά:	Frontiers in Pediatrics
Θέματα:	common variable immunodeficiency granulomatous–lymphocytic interstitial lung disease SOCS1 GLILD inborn errors of immunity
Διαθέσιμο Online:	https://www.frontiersin.org/articles/10.3389/fped.2024.1423858/full
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