Common variable immunodeficiency 10 due to a novel variant of <i>NFKB2</i> and presenting as alopecia universalis and vitiligo
We report an infant patient with common variable immunodeficiency 10 who exhibited a novel variant of NFKB2. Our report emphasizes the importance of genetic testing and long-term follow-up in patients with combined autoimmune manifestations.
Authors
- Bin Zhang (ORCID: https://orcid.org/0000-0002-2970-746X)
- L. Wang (ORCID: https://orcid.org/0000-0003-0788-4876)
Institutions
- Capital Medical University (CN)
- Center for Children (US)
- Beijing Children’s Hospital (CN)
Publication Details
- Journal
- Clinical and Experimental Dermatology
- Published
- 2025-02-05
- DOI
- https://doi.org/10.1093/ced/llaf060
- Primary Topic
- NF-κB Signaling Pathways
- Type
- article
- Field-Weighted Citation Impact
- 0.00