Acanthosis nigricans in a Chinese girl with FGFR3 K650 T mutation: a case report and literature review

• Prif Awduron: Junling Fu (Awdur), Yiting Zhao (Awdur), Tong Wang (Awdur), Qian Zhang (Awdur), Xinhua Xiao (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: BMC, 2019-01-01T00:00:00Z.
• Pynciau: article
• Mynediad Ar-lein: Connect to this object online.

Abstract 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. C...