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  • Poster presentation
  • Open Access

Crouzon Syndrome: a case report

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Journal of Foot and Ankle Research20103 (Suppl 1) :P15

  • Published:


  • Public Health
  • Treatment Option
  • Growth Factor Receptor
  • Genetic Disorder
  • Fibroblast Growth

Crouzon Syndrome is a rare genetic disorder resulting from a mutation of the Fibroblast Growth Factor Receptor 2 Gene. The main presenting feature of this syndrome is craniofacial synostosis but multiple physical dysmorphic features have been reported. There is a dearth of literature detailing the presentation of this syndrome in the foot and lower limb. Therefore, this case report will describe the clinical characteristics of a 22 year old female referred for podiatric assessment. It will also explore the possible treatment options considered for this case.

Authors’ Affiliations

University of East London, London, UK