Department of Hearing Healthcare Profession, Chair of Biophysics, Poznan University of Medical Sciences, Poznań, Poland.
Eur Rev Med Pharmacol Sci. 2020 Aug;24(16):8281-8287. doi: 10.26355/eurrev_202008_22624.
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.
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).
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.
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.
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。
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)。
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。
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。