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低汗型外胚层发育不良患者的全牙缺失。克里斯 - 西门子 - 图赖讷综合征罕见病例报告。

Total anodontia in patient with hypohidrotic ectodermal dysplasia. Report of rare case of Christ-Siemens Touraine syndrome.

作者信息

Sholapurkar Amar A, Setty Suhas, Pai Keerthilatha M

机构信息

Department of Oral Medicine and Radiology, Manipal College of Dental Sciences, Karnataka, India.

出版信息

N Y State Dent J. 2011 Jan;77(1):36-9.

Abstract

Ectodermal dysplasias are a complex group of genetically determined disorders clinically characterized by congenital alterations of the structures derived from the ectoderm. Even though ectodermal dysplasia with partial anodontia is common, this condition with total anodontia is not. We describe features of hypohidrotic ectodermal dysplasia with complete anodontia in a 6-year-old boy. In order to improve esthetics, speech and mastication, the child was provided with upper and lower complete dentures.

摘要

外胚层发育不良是一组复杂的由基因决定的疾病,临床上以源自外胚层的结构先天性改变为特征。尽管伴有部分无牙症的外胚层发育不良很常见,但伴有全部无牙症的情况并不常见。我们描述了一名6岁男孩患有完全无牙症的低汗性外胚层发育不良的特征。为了改善美观、言语和咀嚼功能,为该患儿佩戴了上下全口义齿。

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