...
首页> 外文期刊>The International journal of prosthodontics >Dental Implant Therapy for a Child with X-linked Hypohidrotic Ectodermal Dysplasia-Three Decades of Managed Care
【24h】

Dental Implant Therapy for a Child with X-linked Hypohidrotic Ectodermal Dysplasia-Three Decades of Managed Care

机译:X连锁次同性异基因表皮发育异常的儿童的牙种植体治疗-数十年的照护服务

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose: The aim was to report on oral rehabilitation of a boy with X-linked hypohidrotic ectodermal dysplasia (XLHED) and anodontia of the mandible between ages 3 and 33 years where treatment involved dental implants and oral care management by a multidisciplinary team of specialists. Materials and Methods: This case history report describes the clinical management of a boy born in 1979 with XLHED and anodontia of the mandible. Two implants were successfully placed in the anterior region of the mandible in 1985. Genetic analysis later verified the diagnosis by confirming a mutation in the EDA gene. The case description was based on review of the patient records and assessment of orofacial function. Results: The patient had satisfactory orofacial appearance and function throughout his youth. He is still caries-free at age 33 and has experienced only minor oral complications. Dental management began at age 3, when he received a maxillary removable dental prosthesis. At age 7, he received a mandibular implant-supported overdenture. After two more implants in the mandible and orthodontic treatment in the maxilla, his oral rehabilitation was completed at age 22 with maxillary tooth-supported and mandibular implant-supported fixed dental prostheses. Regular follow-ups provided supervision of oral hygiene, caries prevention, and prosthetic maintenance. Conclusion: This long-term follow-up of a child with XLHED and anodontia in the mandible supports the use of dental implants, with consideration given to the dense bone quality associated with the diagnosis, to establish good orofacial function and appearance from childhood onward.
机译:目的:目的是报告3到33岁之间患有X连锁性多汗症外胚层发育不良(XLHED)和下颌骨缺牙的男孩的口腔康复情况,其中治疗涉及牙科植入物和多学科专家小组的口腔护理管理。材料和方法:本病例历史报告描述了1979年出生的XLHED和下颌骨缺牙的男孩的临床治疗。 1985年,在下颌骨的前部区域成功植入了两枚植入物。遗传分析后来通过确认EDA基因突变来证实诊断。病例描述基于对患者记录的回顾和对口腔功能的评估。结果:患者在整个青年时期都具有令人满意的口腔面部外观和功能。他在33岁时仍然没有龋齿,并且仅经历了轻微的口腔并发症。牙科治疗始于3岁,当时他接受了上颌可移动的假牙。 7岁时,他接受了下颌种植体支持的覆盖义齿。在上颌骨的下颌骨和正畸治疗中再进行两次种植后,他的口腔康复于22岁完成,上颌牙支持和下颌种植体支持的固定义齿修复。定期的随访提供了口腔卫生,龋齿预防和假体维护的监督。结论:对下颌骨患有XLHED和缺牙的儿童进行的长期随访,考虑到与诊断相关的密集骨质,考虑到从儿童期开始就具有良好的口腔功能和外观,这支持使用牙种植体。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号