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Crouzon syndrome: A case report and review of literature
Harroop Kaur1, Harmeet Singh Waraich, Chander Mohan Sharma
1Dept of Opthomology, I.G.Medical College, Shimla.
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 who presented with brachycephaly, maxillary hypoplasia, wide parrot beaked nose, repaired bilateral cleft lip and cleft palate along with dental and orbital abnormalities.
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