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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References
Malcolm S, Reardon W.Fibroblast growth factor receptor-2 mutations in craniosynostosis.Ann NY Acad Sci 1996;785:164–70.
Noetzel MJ, Marsh JL, Palkes H, Gado M.Hydrocephalus & mental retardation in craniosynostosis.J Pediatr 1985;107 (6):885–92.
David Lisa R, Velotta Emily, Weaver R Grey, Wilson John A, Argenta Louis C.Clinical findings precede objective diagnostic testing in the identification of increased intracranial pressure in syndromic craniosynostosis.Journal of Craniofacial Surgery 2002;13(5):676–80.
Carinci F, Avantaggiato A, Curioni C. Crouzon syndrome: Cephalometric analysis and evaluation of pathogenesis.Cleft Palate Craniofac J 1994;31 (3):201–9.
Di Rocco C, Marchese E, Velardi F.Craniosynostosis: surgical treatment during the first year of life.J Neurosurg Sci 1992;36 (3):129–37.
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Kaur, H., Singh Waraich, H. & Sharma, C.M. Crouzon syndrome: A case report and review of literature. Indian J Otolaryngol Head Neck Surg 58, 381–382 (2006). https://doi.org/10.1007/BF03049602
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DOI: https://doi.org/10.1007/BF03049602