Abstract
Crouzon Syndrome (CS) is a rare genetic disorder, due to mutation in Fibroblast Growth Factor Receptor 2 (FGFR2) and Receptor 3 (FGFR3) genes. Clinical features include craniosynostosis, craniofacial malformation, proptosis of the orbits, ocular strabismus, hearing defects, maxillary hypoplasia and mandibular prognathism.
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