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...
| Published in: | Frontiers in Pediatrics |
|---|---|
| Main Authors: | María Soledad Caldirola, Espantoso Daiana, Andrea Cecilia Gomez Raccio, Ana Luz García, Agustin Bernacchia, Martín Medín, Maria Isabel Gaillard, Daniela Di Giovanni |
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2024-06-01
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| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fped.2024.1423858/full |
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