Crouzon Syndrome: a case report
Journal of Foot and Ankle Research volume 3, Article number: P15 (2010)
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.
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Reid, D., Morrison, S. Crouzon Syndrome: a case report. J Foot Ankle Res 3 (Suppl 1), P15 (2010). https://doi.org/10.1186/1757-1146-3-S1-P15