Rabson-Mendenhall syndrome presented as severe acanthosis nigricans in an infant harboring novel mutations in the INSR gene: a case report
Acanthosis nigricans (AN) can serve as a clinical marker that strongly suggests underlying metabolic syndromes, making genetic analysis essential for confirming the diagnosis.
Authors
- Hai-Zhen Hui
- Shi Lin Yan (ORCID: https://orcid.org/0000-0001-8304-8445)
- Yu Sheng (ORCID: https://orcid.org/0000-0001-7356-9343)
- Chunyan Zhou (ORCID: https://orcid.org/0000-0002-5116-2734)
- Deming Liu (ORCID: https://orcid.org/0000-0001-6885-6284)
Institutions
- First People's Hospital of Chongqing (CN)
Publication Details
- Journal
- Frontiers in Pediatrics
- Published
- 2025-04-16
- DOI
- https://doi.org/10.3389/fped.2025.1511429
- Citations
- 1
- Primary Topic
- Skin and Cellular Biology Research
- Type
- article
- Field-Weighted Citation Impact
- 1.15