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Case Studies | Dentistry | Volume 11 Issue 9, September 2022 | Pages: 1115 - 1116 | India
Crouzon Syndrome: A Rare Case Report
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 9, September 2022, International Journal of Science and Research (IJSR), Pages: 1115-1116, https://www.ijsr.net/getabstract.php?paperid=SR22912121255, DOI: https://dx.doi.org/10.21275/SR22912121255