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先天性锁骨颅骨发育不全(CCD)患者的听力学评估。

Audiological evaluation of patients with cleidocranial dysplasia (CCD).

机构信息

Department of Hearing Healthcare Profession, Chair of Biophysics, Poznan University of Medical Sciences, Poznań, Poland.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Aug;24(16):8281-8287. doi: 10.26355/eurrev_202008_22624.

Abstract

OBJECTIVE

The description of clinical manifestation of hearing problems in cleidocranial dysplasia (CCD) remains limited and incomplete, since CCD constitutes a rare congenital disorder. The study aims to provide a complex panel analysis of the auditory system in patients suffering from the disease.

PATIENTS AND METHODS

The study group consisted of 4 children with CCD (aged: 12-15), who underwent orthodontic treatment. A full panel analysis of their auditory systems was performed, including high-frequency audiometry and a new method of middle ear assessment - WBT (Wideband Tympanometry).

RESULTS

A slight conductive hearing loss was diagnosed in 3 out of 4 patients. While high frequency audiometry has shown a deterioration of hearing in 3 patients, in one case, the obtained thresholds were within the normal range. A decrease of absorbance in low frequencies has been observed in one or both ears. Only one patient has had a shift of maximum absorbance towards high frequencies in the left ear.

CONCLUSIONS

The presented manuscript is the first with a complete evaluation of the auditory system comprising 4 cases of children in a similar age group. All of the examined patients presented an air-bone gap indicating conductive disorders.

摘要

目的

由于颅锁骨发育不全(CCD)是一种罕见的先天性疾病,因此对其听力问题临床表现的描述仍然有限且不完整。本研究旨在对患有该病的患者的听觉系统进行复杂的综合分析。

患者和方法

研究组包括 4 名患有 CCD(年龄:12-15 岁)的儿童,他们接受了正畸治疗。对他们的听觉系统进行了全面的分析,包括高频测听和中耳评估的新方法 - WBT(宽带鼓室图)。

结果

4 名患者中有 3 名被诊断为轻度传导性听力损失。虽然高频测听显示 3 名患者的听力恶化,但在 1 名患者中,获得的阈值在正常范围内。在一只或两只耳朵中观察到低频吸收率下降。只有 1 名患者的左耳最大吸收率向高频转移。

结论

本文是第一篇对包括 4 名年龄相似的儿童在内的听觉系统进行全面评估的论文。所有接受检查的患者均存在提示传导性障碍的气骨导差。

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