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April 23, 2026Frontiers in ImmunologyOpen Access

Correction: IL2RG-related immunodeficiencies: from SCID to atypical presentations

Efrossini Briassouli Nikolaos Marinakis Vana Spoulou Luigi DNotarangelo

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Key Points

This correction addresses issues related to the representation of figure content in the original publication.
Identification of mistakes in Figure 1.
Adherence to Creative Commons licensing for figures and illustrations.
Communication with the journal's editorial office regarding publication standards.
Clarification of responsibilities for obtaining permissions for copyrighted material.
Ensured proper citation instructions are followed for third-party content.

Implication

Correction confirms figure accuracy in IL2RG immunodeficiency presentations, ensuring reliable data representation.

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Cite This Study

Briassouli et al. (2026) studied this question.

synapsesocial.com/papers/69eefc23fede9185760d3668 https://doi.org/10.3389/fimmu.2026.1839148

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Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1A novel de novo IL2RG nonsense mutation in a pediatric patient with X-linked severe combined immunodeficiency2025 · 1 citations
2Novel <i>IL2RB</i> gene defect associated with severe eczema, recurrent infections, lymphoproliferation, and <scp>IgA</scp> nephropathy2024
3Case Report and literature review: X-linked severe combined immunodeficiency complicated by Talaromyces marneffei infection caused by a novel pathogenic IL2RG mutationCase Report · 2026
4Novel Pathogenic Variant in IL2RG Affecting the Signal Peptide Results in mRNA Instability, Decreased IL2RG Expression, and Atypical Late-Onset Immunodeficiencycase_report · 2026
5Atypical presentation of <i>RAG1</i>-associated SCID: diagnostic challenges beyond infections and lymphocyte countOriginal Research · 2026

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Clinical Manifestations and Immunologic Phenotype in Patients With RAG1/2 Mutations: A Single Centre Experience and Description of A Novel Mutation2026
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Correction: First review of chronic granulomatous disease in Palestine: clinical and genetic characteristics2026

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