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Article

Cutaneous features of Crouzon syndrome with acanthosis nigricans.

JAMA dermatology - 1 Jun 2013

Mir Adnan, Wu Timothy, Orlow Seth J

Abstract excerpt

IMPORTANCE: Crouzon syndrome with acanthosis nigricans is a distinct disorder caused by a mutation in the FGFR3 gene, featuring craniosynostosis, characteristic facial features, and atypical and extensive acanthosis nigricans. Other cutaneous findings have not been thoroughly described. OBSERVATIONS: We report 6 cases and summarize the existing literature with regard to the cutaneous manifestations of this...

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Source

Identifiers

PMID: 23571469
DOI: 10.1001/jamadermatol.2013.3019

Genes

FGFR3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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