Abstract :
Crouzon syndrome is a rare congenital malformation of cranium and face. It is an autosomal dominant disorder characterized by premature fusion (craniosynostosis) of coronal and sagittal sutures leading to craniodentofacial deformities. We report here a case of 5 year old female with ocular, skeletal and dental features of Crouzon syndrome.
Keyword :
Craniosynostosis, Crouzon syndrome, Exophthalmos, FGFR 2 gene mutation, Prognathism.