Crouzon Syndrome: A Rare Case Report

Poornima Tripathi, Sonal Gupta, Sakshi Patel

Abstract: Crouzon syndrome also called craniofacial dysostosis is an autosomal dominant disorder characterized by premature closure of cranial sutures, midfacial hypoplasia, and orbital defects. Herein we report a case of this rare entity with Ectomorphic body shape, Exophthalmoses eyes, Flat broad nasal bridge, and low set ears.

Keywords: Craniofacial dysostosis, crouzon syndrome, copper beaten appearance, exophthalmos