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Crouzon syndrome-acanthosis nigricans syndrome

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Description

Crouzon syndrome with acanthosis nigricans is considered to be a distinct disorder from classic Crouzon syndrome (123500), which is caused by mutation in the FGFR2 gene (176943). Cohen (1999) argued that this condition is separate from Crouzon syndrome for 2 main reasons: it is caused by a highly specific mutation of the FGFR3 gene, whereas multiple different FGFR2 mutations result in Crouzon syndrome, and the phenotypes are different.

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

13

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Genes

External Links

  • OMIM

    612247

  • Orphanet

    93262

  • HPO
  • Medgen

    C2677099

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