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IP International Journal of Ocular Oncology and Oculoplasty

Crouzon Syndrome: A case report with review of literature

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Author Details: Priyanshi Awasthi, Rajendra P. Maurya, Virendra P. Singh, Tanmay Srivastav

Volume : 3

Issue : 4

Online ISSN : 2581-5016

Print ISSN : 2581-5024

Article First Page : 316

Article End Page : 317


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.

Keywords: Craniosynostosis, Crouzon syndrome, Exophthalmos, FGFR 2 gene mutation, Prognathism.