Early orthodontic management of Crouzon Syndrome: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Otorhinolaryngology,Oral Surgery,Surgery
Link
http://link.springer.com/content/pdf/10.1007/s12663-009-0018-7.pdf
Reference7 articles.
1. Fogh-Andersen P (1943) Craniofacial dysostosis (Crouzon’s disease) as a dominant hereditary affection. Nord Med 18: 993–996
2. Crouzon O (1912) Dysostose craniofaciale hereditaire. Bull Mem Soc Med Hosp Paris 33: 545–555
3. Fries PD, Katowitz JA (1990) Congenital craniofacial anomalies of ophthalmic importance. Surv Ophthalmol 35(2): 87–119
4. Cohen MM Jr (1988) Craniosynostosis update 1987. Am J Med Genet Suppl 4: 99–148
5. Cohen MM Jr, Kreiborg S (1992) Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methods. Clin Genet 41(1): 12–15
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