Literature DB >> 7937257

Williams syndrome--oral presentation of 45 cases.

J Hertzberg1, L Nakisbendi, H L Needleman, B Pober.   

Abstract

Forty-five patients with Williams syndrome (WS) were evaluated for oral abnormalities. The mean age of the patients was 9.25 years, the median age was 6.7 years, and the majority (62.2%) were male. Hypodontia was present in 11.1% of the patients. Abnormal tooth morphology was noted in 12.5% of the primary dentitions and 40.7% of the permanent dentitions. With the exception of the primary mandibular central incisors of males, all mesiodistal incisor crown dimensions were statistically significantly smaller when compared with norms (P < 0.05). At least one hypoplastic enamel defect was present in 9.4% of patients with primary teeth and in 18.5% with permanent teeth. No patients exhibited generalized enamel hypoplasia. More than half of the patients (59.1%) were both caries and restoration free, while only 13.6% presented with clinically active caries. Tongue thrusting was present in 67.7% of the sample, while more than 50% of the patients present with excessive interdental spacing. Patients exhibited a higher than normal prevalence of Class II and III occlusions, open and deep bites and anterior crossbites. No single dental finding was pathognomonic of WS, however two constellations of findings, each occurring in approximately one-third of the sample, were observed: 1) microdontia, anterior crossbite, tongue thrusting, and excessive interdental spacing, and 2) microdontia, deep or open bite, and excessive interdental spacing.

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Mesh:

Year:  1994        PMID: 7937257

Source DB:  PubMed          Journal:  Pediatr Dent        ISSN: 0164-1263            Impact factor:   1.874


  7 in total

1.  Alternative treatment for open bite Class III malocclusion in a child with Williams-Beuren syndrome.

Authors:  Giovanni Modesto Vieira; Eduardo Jacomino Franco; Denise Falcão Pinheiro da Rocha; Laudimar Alves de Oliveira; Rivadávio Fernandes Batista Amorim
Journal:  Dental Press J Orthod       Date:  2015 Jan-Feb

2.  Dental age estimation in children with chromosomal syndromes

Authors:  V Pinchi; G Vitale; F Pradella; L Farese; M Focardi
Journal:  J Forensic Odontostomatol       Date:  2018-05-30

3.  Dentofacial characteristics in William's syndrome.

Authors:  P Poornima; Piyusha S Patil; V V Subbareddy; Geetika Arora
Journal:  Contemp Clin Dent       Date:  2012-04

4.  Orthodontic Treatment and Maxillary Anterior Segmental Distraction Osteogenesis of a Subject with Williams-Beuren Syndrome and Isolated Cleft Palate: A Long-Term Follow-Up from the Age of 5 to 24 Years.

Authors:  Tetsutaro Yamaguchi; Tatsuo Shirota; Mohamed Adel; Masahiro Takahashi; Shugo Haga; Ryo Nagahama; Misato Nakashima; Mayu Furuhata; Takaaki Kamatani; Koutaro Maki
Journal:  Case Rep Dent       Date:  2017-07-04

5.  Claudin Loss-of-Function Disrupts Tight Junctions and Impairs Amelogenesis.

Authors:  Claire Bardet; Sandy Ribes; Yong Wu; Mamadou Tidiane Diallo; Benjamin Salmon; Tilman Breiderhoff; Pascal Houillier; Dominik Müller; Catherine Chaussain
Journal:  Front Physiol       Date:  2017-05-24       Impact factor: 4.566

6.  Oral findings in Williams-Beuren syndrome.

Authors:  S-B-P Ferreira; M-M Viana; N-G-F Maia; L-L Leão; R-A Machado; R-D Coletta; M-J-B de Aguiar; H Martelli-Júnior
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2018-01-01

Review 7.  Williams syndrome.

Authors:  Beth A Kozel; Boaz Barak; Chong Ae Kim; Carolyn B Mervis; Lucy R Osborne; Melanie Porter; Barbara R Pober
Journal:  Nat Rev Dis Primers       Date:  2021-06-17       Impact factor: 65.038

  7 in total

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