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Acanthosis nigricans in a Chinese girl with FGFR3 K650 T mutation: a case report and literature review
BACKGROUND: Acanthosis nigricans (AN) is a clinical manifestation featured by velvety brown plaques in skin folds that occurs in some hereditary and syndromic disorders. Fibroblast growth factor receptor 3 (FGFR3) mutations have been identified as one of the genetic causes of inherited AN. CASE PRES...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329052/ https://www.ncbi.nlm.nih.gov/pubmed/30635042 http://dx.doi.org/10.1186/s12881-019-0748-4 |