Crouzon Syndrome: a case report

Article

Reid, David and Morrison, Stuart 2010. Crouzon Syndrome: a case report. Journal of Foot and Ankle Research. 3 (Suppl), p. P15.
AuthorsReid, David and Morrison, Stuart
Abstract

Crouzon Syndrome is a rare genetic disorder resulting
from a mutation of the Fibroblast Growth Factor Recep-
tor 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.

JournalJournal of Foot and Ankle Research
Journal citation3 (Suppl), p. P15
ISSN1757-1146
Year2010
PublisherBioMed Central
Publisher's version
License
CC BY
Web address (URL)http://dx.doi.org/10.1186/1757-1146-3-S1-P15
Publication dates
Print20 Dec 2010
Publication process dates
Deposited13 Mar 2015
Copyright information© 2013 Watts et al. 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 author and source are credited.
Additional information

Poster was presented at Society of Chiropodists and Podiatrists Annual Conference 2010 (Bournemouth, UK. 21-23 October 2010)

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