一名患有Usher综合征并植入人工耳蜗的儿童出现牙釉质缺陷和异位萌出。
Enamel defects and ectopic eruption in a child with Usher syndrome and a cochlear implant.
作者信息
Balmer Richard, Fayle Stephen A F
机构信息
Division Child Dental Health, Leeds Dental Institute, Leeds, UK.
出版信息
Int J Paediatr Dent. 2007 Jan;17(1):57-61. doi: 10.1111/j.1365-263X.2006.00778.x.
BACKGROUND
Usher syndrome is a genetic disorder consisting of progressive loss of vision and hearing.
CASE REPORT
The paper describes an 8-year-old girl with Usher syndrome type I who presented with generalized defects of the permanent dentition and ectopic eruption of the right maxillary first permanent molar. A cochlear implant had been fitted for her hearing loss, and the report reviews the implications of this device for dental treatment. The impacted first permanent molar was encouraged to erupt into the correct position by shaving the distal surface of the second primary molar.
CONCLUSION
This is the first report to describe in detail an association between Usher syndrome and enamel defects.
背景
尤塞氏综合征是一种遗传性疾病，表现为视力和听力进行性丧失。
病例报告
本文描述了一名患有I型尤塞氏综合征的8岁女孩，其恒牙列出现广泛性缺损，右上颌第一恒磨牙异位萌出。她因听力损失植入了人工耳蜗，本报告探讨了该装置对牙科治疗的影响。通过磨除第二乳磨牙的远中面，促使阻生的第一恒磨牙萌出到正确位置。
结论
这是首份详细描述尤塞氏综合征与牙釉质缺陷之间关联的报告。
Zotero 插件