Crouzon syndrome: A case report and review of literature
Author:
Publisher
Springer Science and Business Media LLC
Subject
Otorhinolaryngology,Surgery
Link
http://link.springer.com/content/pdf/10.1007/BF03049602.pdf
Reference5 articles.
1. Malcolm S, Reardon W.Fibroblast growth factor receptor-2 mutations in craniosynostosis.Ann NY Acad Sci 1996;785:164–70.
2. Noetzel MJ, Marsh JL, Palkes H, Gado M.Hydrocephalus & mental retardation in craniosynostosis.J Pediatr 1985;107 (6):885–92.
3. 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.
4. Carinci F, Avantaggiato A, Curioni C. Crouzon syndrome: Cephalometric analysis and evaluation of pathogenesis.Cleft Palate Craniofac J 1994;31 (3):201–9.
5. 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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