eng Science and Education Publishing American Journal of Medical Case Reports 2374-216X 2021-01-19 9 4 213 215 10.12691/ajmcr-9-4-2 AJMCR2021942 article Mohammed Al Homsi 1 Ammar Al Homsi Mohammadalhomsi84@gmail.com 1 Malay Jhancy 2 RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras al Khaimah, United Arab Emirates Pediatrics, RAK Medical and Health Sciences University, Ras al Khaimah, United Arab Emirates 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. http://pubs.sciepub.com/ajmcr/9/4/2/ajmcr-9-4-2.pdf Crouzon¡¯s syndrome craniosynostosis maxillary hypoplasia