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...

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Detalles Bibliográficos
Autores principales: Fu, Junling, Zhao, Yiting, Wang, Tong, Zhang, Qian, Xiao, Xinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
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

Internet

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

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