@article{ajmcr2021942,
author={{Homsi, Mohammed Al and Homsi, Ammar Al and Jhancy, Malay},
title={Crouzon¡¯s Syndrome: A Case Report},
journal={American Journal of Medical Case Reports},
volume={9},
number={4},
pages={213--215},
year={2021},
url={http://pubs.sciepub.com/ajmcr/9/4/2},
issn={2374-216X},
abstract={Crouzon¡¯s syndrome is a rare autosomal dominant disorder characterized by craniofacial malformations. It¡¯s the most common syndrome among the craniosynostosis group accounting for about 4.8 % of all of them. Crouzon syndrome is caused by mutation in the fibroblast growth factor receptor-2 (FGFR-2) gene resulting in premature closure of suture lines. Our article describes a case report of a 3 years old girl who displayed characteristic dysmorphic skull and facial features of Crouzon¡¯s syndrome.},
doi={10.12691/ajmcr-9-4-2}
publisher={Science and Education Publishing}
}