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...
में बचाया:
| मुख्य लेखकों: | , , , , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Frontiers Media S.A.
2024-06-01
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| श्रृंखला: | Frontiers in Pediatrics |
| विषय: | |
| ऑनलाइन पहुंच: | https://www.frontiersin.org/articles/10.3389/fped.2024.1423858/full |
| टैग: |
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