首页> 外文期刊>Audiological medicine >An audio-vestibular study of 128 children presenting to a specialized paediatric audio-vestibular clinic: Should every child with hearing impairment have vestibular function assessed?
【24h】

An audio-vestibular study of 128 children presenting to a specialized paediatric audio-vestibular clinic: Should every child with hearing impairment have vestibular function assessed?

机译:一项针对128名儿童的听觉-听觉研究,就诊于专门的儿科听觉-听觉诊所:是否应该对每个听力障碍的儿童进行前庭功能评估?

获取原文
获取原文并翻译 | 示例
           

摘要

This is a study of the vestibular function of 128 children with a varying degree/type and cause of hearing impairment presenting to a specialized paediatric vestibular service. It shows that there are some syndromic and non-syndromic conditions that may be associated with vestibular dysfunction. Due to the relatively small cohort of children tested with a lesser degree of hearing impairment, the study is unable to confirm the proportional dependence of the presence of vestibular dysfunction with the degree of hearing impairment but it confirms such a trend. However, it supports earlier findings that profound hearing loss due to autosomal recessive inheritance associated with mutation in the Connexin 26 gene is not associated with vestibular dysfunction of the lateral semicircular canal. It further shows that children with profound hearing loss and lack of vestibular function present with a history of gross motor developmental delay. It argues that the referral of a child for vestibular assessment should be based on the knowledge of syndromicon-syndromic conditions associated frequently with inner ear anomalies as well as the knowledge of the noxious factors that may lead to vestibular dysfunction and also hearing impairment such as meningitis, rubella, birth risk factors and ototoxicity.
机译:这是一项针对128名不同程度/类型和听力障碍原因的儿童的前庭功能的研究,这些儿童出现在专门的儿科前庭服务中。它表明存在一些综合征和非综合征性疾病,可能与前庭功能障碍有关。由于接受测试的儿童相对较少,听力障碍程度较小,因此该研究无法确定前庭功能障碍的存在与听力障碍程度的比例依赖性,但证实了这种趋势。但是,它支持更早的发现,即与连接蛋白26基因突变相关的常染色体隐性遗传导致的严重听力损失与外侧半规管的前庭功能障碍无关。它进一步表明,患有严重听力损失和前庭功能不足的儿童存在严重的运动发育迟缓史。它认为,将儿童转介到前庭评估应基于与内耳异常经常相关的综合症/非综合症的知识,以及可能导致前庭功能障碍和听力障碍的有害因素的知识。如脑膜炎,风疹,出生危险因素和耳毒性。

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