克里斯蒂·西门子·图赖讷综合征：两例报告及假体管理的恰当方法
Christ Siemens Touraine syndrome: Two case reports and felicitous approaches to prosthetic management.
作者信息
Renahan Navanith, Raj Renju, Varma R Balagopal, Kumar J Suresh
机构信息
Department of Pedodontics and Preventive Dentistry, Amrita School of Dentistry, Kochi, Kerala, India.
出版信息
Contemp Clin Dent. 2015 Apr-Jun;6(2):274-6. doi: 10.4103/0976-237X.156066.
Ectodermal dysplasia is a heterogeneous group of inherited disorders, which exhibit a classic triad of hypohydrosis, hypotrichosis, and hypodontia. Hypohidrotic or anhidrotic ectodermal dysplasia or Christ Siemens Touraine syndrome is the most common condition among ectodermal dysplasia patients. This is a case report on two Christ Siemens Touraine syndrome cases and two different approaches to prosthetic management.
外胚层发育不良是一组遗传性疾病的异质性群体，表现为少汗、少毛和缺牙的典型三联征。少汗型或无汗型外胚层发育不良或克里斯·西门子·图赖讷综合征是外胚层发育不良患者中最常见的病症。本文是关于两例克里斯·西门子·图赖讷综合征病例及两种不同修复治疗方法的病例报告。
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