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  • 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


© Reid and Morrison; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.