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先天性后鼻孔闭锁与神经性耳聋。

Congenital choanal atresia and nerve deafness.

作者信息

Brama I, Engelhard D

出版信息

J Laryngol Otol. 1979 Dec;93(12):1223-8. doi: 10.1017/s0022215100088332.

Abstract

Four cases of bilateral congenital choanal atresia are presented. Three of them (75 per cent) were shown by Electric Response Audiometry (ERA) tests to have, in addition, congenital nerve deafness; and two had other congenital anomalies. Thus, congenital nerve deafness should be considered as a possible congenital anomaly associated with choanal atresia. Early diagnosis and treatment of congenital choanal atresia can prevent death from asphyxia during the neonatal period, but after surgical correction of the atresia the possible existence of additional anomalies has to be determined and treated. By the use of electric response audiometry we are able to detect sensorineural hearing loss during the neonatal period and can plan the rehabilitation of deaf infants.

摘要

本文报告了4例双侧先天性后鼻孔闭锁病例。其中3例(75%)经电反应测听(ERA)测试显示还患有先天性神经性耳聋;2例伴有其他先天性异常。因此,先天性神经性耳聋应被视为与后鼻孔闭锁相关的一种可能的先天性异常。先天性后鼻孔闭锁的早期诊断和治疗可预防新生儿期因窒息死亡,但在闭锁手术矫正后,必须确定并治疗可能存在的其他异常。通过使用电反应测听,我们能够在新生儿期检测出感音神经性听力损失,并可为失聪婴儿制定康复计划。

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