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患有特雷彻·柯林斯综合征的受试者中牙齿异常、异位萌出及相关口腔畸形的患病率。

Prevalence of dental anomalies, ectopic eruption and associated oral malformations in subjects with Treacher Collins syndrome.

作者信息

da Silva Dalben Gisele, Costa Beatriz, Gomide Marcia Ribeiro

机构信息

Public Health Dentistry Sector, Hospital for Rehabilitation of Craniofacial Anomalies of University of São Paulo, Bauru, SP, Brazil.

出版信息

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006 May;101(5):588-92. doi: 10.1016/j.tripleo.2005.07.016. Epub 2006 Feb 17.

Abstract

OBJECTIVE

To examine the prevalence of dental anomalies in the deciduous and permanent teeth, ectopic eruption of permanent first molars, and associated oral malformations in individuals with Treacher Collins syndrome.

STUDY DESIGN

Clinical and radiographic examination of 15 patients with Treacher Collins syndrome, from the Hospital for Rehabilitation of Craniofacial Anomalies of the University of São Paulo, not submitted to orthodontic or orthognathic treatment.

RESULTS

Dental anomalies were present in 60% of the sample, with 1-8 anomalies per individual. Hypoplastic dental anomalies were the most common, followed by heterotopic and hyperplastic dental alterations. The most frequent anomalies were tooth agenesis (33.3%), mainly affecting the mandibular second premolars, and enamel opacities (20% of patients). Ectopic eruption of the maxillary first molars was found in 13.3% of subjects. Associated oral malformations, primarily isolated cleft palate, followed by complete cleft lip and palate and macrostomia, were observed in 66.7% of patients.

CONCLUSIONS

Presence of cleft palate associated with the syndrome is in agreement with the literature. The high prevalence of dental anomalies suggests a possible etiologic relationship, not described in the literature so far, between such alterations and the Treacher Collins syndrome. Further investigations on larger samples are required to confirm these results.

摘要

目的

研究患有特雷彻·柯林斯综合征个体的乳牙和恒牙牙列异常、恒牙第一磨牙异位萌出及相关口腔畸形的患病率。

研究设计

对来自圣保罗大学颅面畸形康复医院的15例未经正畸或正颌治疗的特雷彻·柯林斯综合征患者进行临床和影像学检查。

结果

60%的样本存在牙列异常,每人有1至8种异常。牙发育不全异常最为常见,其次是异位和增生性牙齿改变。最常见的异常是牙齿缺失(33.3%),主要影响下颌第二前磨牙,以及釉质混浊(占患者的20%)。13.3%的受试者出现上颌第一磨牙异位萌出。66.7%的患者存在相关口腔畸形,主要是孤立性腭裂,其次是完全性唇腭裂和巨口症。

结论

与该综合征相关的腭裂的存在与文献报道一致。牙列异常的高患病率表明,迄今为止文献中未描述的此类改变与特雷彻·柯林斯综合征之间可能存在病因学关系。需要对更大样本进行进一步研究以证实这些结果。

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