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

How to Cite?: Poornima Tripathi, Sonal Gupta, Sakshi Patel, "Crouzon Syndrome: A Rare Case Report", Volume 11 Issue 10, October 2022, International Journal of Science and Research (IJSR), Pages: 93-96, https://www.ijsr.net/getabstract.php?paperid=SR22929024100, DOI: https://dx.doi.org/10.21275/SR22929024100