Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Orofacial Findings and Dental Management of Williams-Beuren Syndrome
1Pediatric Dentistry Posgraduate Program, Facultad de Estomatología, Universidad Autónoma de San Luis Potosí, México.
DOI: 10.17796/jcpd.36.4.c93436771101tm06 Vol.36,Issue 4,July 2012 pp.401-404
Published: 01 July 2012
*Corresponding Author(s): Pozos-Guillén AJ E-mail: apozos@uaslp.mx.
Williams-Beuren syndrome is a rare congenital disorder involving the cardiovascular system, mental retardation, distinctive facial features, and tooth anomalies. The aim of the present report is to show a 10-yearold girl with Williams-Beuren syndrome, her general and orofacial clinical characteristics and the dental management.
Williams-Beuren syndrome
Campos-Lara P,Santos-Diaz MA,Ruiz-Rodríguez MS,Garrocho-Rangel JA,Pozos-Guillén AJ. Orofacial Findings and Dental Management of Williams-Beuren Syndrome. Journal of Clinical Pediatric Dentistry. 2012. 36(4);401-404.
1. Axelsson S, Bjørnland T, Kjaer I, Heiberg A, Storhaug K. Dental characteristics in Williams syndrome: A clinical and radiographic evaluation. Acta Odontol Scand, 61: 129–136, 2003.
2. Williams JC, Barratt-Boyes BG, Lowe JB. Supravalvular aortic stenosis. Circulation, 24: 1311–1318, 1961.
3. Beuren AJ, Apitz J, Harmjanz D. Supravalvular aortic stenosis in association with mental retardation and a certain facial appearance. Circulation, 26: 1235–1240, 1962.
4. Donnai D, Karmiloff-Smith A. Williams syndrome: From genotype through to the cognitive phenotype. Am J Med Genet, 97: 164–171, 2000.
5. Morris CA, Mervis CB. Williams syndrome and related disorders. Ann Rev Genomics Hum Genet, 1: 461–484, 2000.
6. Hertzberg J, Nakisbendi L, Needleman HL, Pober B. Williams syndrome—Oral presentation of 45 cases. Pediatr Dent, 16: 262–267, 1994.
7. Kashyap AS, Sharma HS, Kumar P. Dental anomalies in Williams syndrome. Postgrad Med J, 76: 712, 2000.
8. Trajan I, Balaton G, Balaton P, Varbiro S, Vajo Z. Facial and dental appearance of Williams syndrome. Postgrad Med J, 79: 241, 2003.
9. Morris CA, Demsey SA, Leonard CO, Dilts C, Blackburn BL. Natural history of Williams syndrome: Physical characteristics. J Pediatr, 113: 318–326, 1988.
10. Strømme P, Bjørnstad PG, Ramstad K. Prevalence estimation of Williams syndrome. J Child Neurol, 17: 269–271, 2002.
11. Sadler LS, Robinson LK, Verdaasdonk KR, Gingell R. The Williams syndrome: Evidence for possible autosomal dominant inheritance. Am J Med Genet, 47: 468–470, 1993.
12. Ohazama A, Sharpe PT. TFII-I gene family during tooth development: Candidate genes for tooth anomalies in Williams syndrome. Dev Dyn, 236: 2884–2888, 2007.
13. Udwin O, Yule W. A cognitive and behavioural phenotype in Williams syndrome. J Clin Exp Neuropsychol, 13: 232–244, 1991.
14. Committee on Genetics. American Academy of Pediatrics: Health care supervision for children with Williams syndrome. Pediatrics, 107: 1192–1204, 2001.
15. Morris CA, Mervis CB, Hobart HH, Gregg RG, Bertrand J, Ensing GJ, Sommer A, Moore CA, Hopkin RJ, Spallone PA, Keating MT, Osborne L, Kimberley KW, Stock AD. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype-phenotype analysis of five families with deletions in the Williams syndrome region. Am J Med Genet, 123A: 45–59, 2003.
16. Boraz RA. Williams (Elfin Facies) syndrome: Review of the literature and report of a rare case. ASDC J Dent Child, 58: 57–59, 1991.
17. Onçag A, Gunbay S, Parlar A. Williams syndrome. J Clin Pediatr Dent, 19: 301–304, 1995.
18. Knudtzon J, Aksnes L, Akslen LA, Aaskog D. Elevated 1,25-dihydroxyvitamin D and normocalcemia presumed familiar Williams syndrome. Clin Genet, 32: 369–374, 1987.
19. Cobo J, Argüelles J, Vijande M, Ibaseta G. Williams syndrome. Report of a case. Oral Surg Oral Med Oral Pathol, 74: 756–759, 1992.
Top