Ferreira SBP, Viana MM, Maia NGF, Leão LL, Machado RA, Coletta RD, de Aguiar MJB, Martelli-Júnior H. Oral ndings in Williams-Beuren syndrome. Med Oral Patol Oral Cir Bucal. 2018 Jan 1;23 (1):e1-6.

doi:10.4317/medoral.21834

http://dx.doi.org/doi:10.4317/medoral.21834

1. On-line Mendelian Inheritance in Man, OMIM (TM) Johns Hopkins University, Baltimore, MD. MIM Number: 194050. Edited 2016 Aug 9. Accessed 2016 Dec 12. Available from: http//www.ncbi.nlm.nih.gov/omim/

2. Strøme P, Bjornstad P, Ramstad K. Prevalence estimation of Williams syndrome. J Child Neurol. 2002;17:269–271. https://doi.org/10.1177/088307380201700406 PMid:12088082

3. American Academy of Pediatrics (Committee on Genetics). Health Care Supervision for Children with Williams Syndrome. Pediatrics. 2001;107:1192-1204. PMid:11331709

4. Morris CA. Introduction: Williams Syndrome. Am J Med Genet C Semin Med Genet. 2010;154C:203-208. https://doi.org/10.1002/ajmg.c.30266 PMid:20425781 PMCid:PMC2946897

5. Morris CA, Loker J, Ensing G, Stock AD. Supravalvular aortic stenosis cosegregates with a familial 6:7 translocation which disrupts the elastin gene. Am J Med Genet. 1993;46:737-744. https://doi.org/10.1002/ajmg.1320460634 PMid:8362925

6. Yau EKC, Lo, IFM, Lam STS. Williams-Beuren syndrome in the Hong Kong Chinese population: retrospective study. Hong Kong Med J. 2004;10:22-27. PMid:14967851

7. Dutra RL, Honjo RS, Kulikowski LD, Fonseca FM, Pieri PC, Jehee FS, et al. Copy number variation in Williams-Beuren syndrome: suitable diagnostic strategy for developing countries. BMC Res Notes. 2012;5:13-17. https://doi.org/10.1186/1756-0500-5-13 PMid:22226172 PMCid:PMC3285034

8. Patil S, Rao RS, Majumdar B. Chromosomal and Multifactorial Genetic Disorders with Oral Manifestations. J Int Oral Health. 2014;6:118-125. PMid:25395808 PMCid:PMC4229819

9. Joyce CA, Zorich B, Pike SJ, Barber JC, Dennis NR. Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patients. J Med Genet. 1996;33:986-992. https://doi.org/10.1136/jmg.33.12.986 PMid:9004128 PMCid:PMC1050807

10. Ewart AK, Morris CA, Atkinson D, Jin W, Sternes K, Spallone P, et al. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nat Genet. 1993;5:11-16. https://doi.org/10.1038/ng0993-11 PMid:7693128

11. Colleen A, Morris MD. Williams syndrome and related desorders. Colleen A. Morris, M.D. Annu. Rev Genomics Hum Genet. 2000;1:461–484. https://doi.org/10.1146/annurev.genom.1.1.461 PMid:11701637

12. Viana MM, Stofanko M, Gonçalves-Dornelas H, Cunha PdS, Aguiar MJB. Phenotype of Williams–Beuren syndrome in Brazilian patients: Comments on the article by Patil et al. [2012] and discussion of variable phenotypes in distinct populations. Am J Med Genet Part A. 2013;161A:637-638. https://doi.org/10.1002/ajmg.a.35740 PMid:23349022

13. Moskovitz M, Brener D, Faibis S, Peretz B. Medical considerations in dental treatment of children with Williams syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;99:573-580. https://doi.org/10.1016/j.tripleo.2004.03.019 PMid:15829880

14. Torres CP, Valadares G, Martins MI, Borsatto MC, Díaz-Serrano KV, de Queiroz AM. Oral findings and dental treatment in a child with Williams-Beuren syndrome. Braz Dent J. 2015;26:312-316. https://doi.org/10.1590/0103-6440201300335 PMid:26200160

15. Habersack K, Grimaldi B, Paulus GW. Orthodontic orthognathic surgical treatment of a subject with Williams Beuren syndrome a follow-up from 8 to 25 years of age. Eur J Orthod. 2007;29:332-337. https://doi.org/10.1093/ejo/cjm031 PMid:17702793

16. Axelsson S, Bjørnland T, Kjaer I, Heiberg A, Storhaug K. Dental characteristics in Williams syndrome: a clinical and radiographic evaluation. Acta Odontol Scand. 2003;61:129-136. https://doi.org/10.1080/00016350310001451 PMid:12868685

17. Hertzberg J, Nakisbendi L, Needleman HL, Pober B. Williams syndrome-oral presentation of 45 cases. Pediatr Dent. 1994;16:262-267. PMid:7937257

18. Vieira GM, Franco EJ, Rocha DFP, Oliveira LA, Amorim RFB. Alternative treatment for open bite Class III malocclusion in a child with Williams-Beuren syndrome. Dental Press J Orthod. 2015;20:97-107. https://doi.org/10.1590/2176-9451.20.1.097-107.oar PMid:25741831 PMCid:PMC4373022

19. Ferrari Júnior FM, Ayub PV, Capelozza Filho L, Pereira Lauris JR, Garib DG. Esthetic evaluation of the facial profile in rehabilitated adults with complete bilateral cleft lip and palate. J Oral Maxillofac Surg. 2015;73:169.e1-6. https://doi.org/10.1016/j.joms.2014.09.012 PMid:25511967

20. Ohazama A, Sharpe PT. TFII-I gene family during tooth development: candidate genes for tooth anomalies in Williams syndrome. Dev Dyn. 2007;236:2884-2888. https://doi.org/10.1002/dvdy.21311 PMid:17823943

21. Fusco C, Micale L, Augello B, Teresa Pellico M, Menghini D, Alfieri P, Cristina Digilio M, Mandriani B, Carella M, Palumbo O, Vicari S, Merla G. Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits. Eur J Hum Genet. 2014;22:64-70. https://doi.org/10.1038/ejhg.2013.101 PMid:23756441 PMCid:PMC3865388