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温度敏感性听觉神经病所致的短暂性耳聋。

Transient deafness due to temperature-sensitive auditory neuropathy.

作者信息

Starr A, Sininger Y, Winter M, Derebery M J, Oba S, Michalewski H J

机构信息

House Ear Institute, Los Angeles, California, USA.

出版信息

Ear Hear. 1998 Jun;19(3):169-79. doi: 10.1097/00003446-199806000-00001.

Abstract

OBJECTIVE

To define mechanisms accounting for transient deafness in three children (two siblings, ages 3 and 6, and an unrelated child, age 15) when they become febrile.

DESIGN

Audiometric tests (pure-tone audiometry, speech and sentence comprehension), tympanometry, middle ear muscle reflex thresholds, otoacoustic emissions (OAEs), and electrophysiological methods (auditory brain stem responses [ABRs], sensory evoked potentials, peripheral nerve conduction velocities) were used to test the children when they were afebrile and febrile.

RESULTS

ABRs, when afebrile, were abnormal with a profound delay of the IV-V and absence of waves I-III. The ABR in one of the children, tested when febrile, showed no ABR components. Measures of cochlear receptor function using OAEs were normal in both febrile and afebrile states. Cochlear microphonic potentials were present in the three children, and a summating potential was likely present in two. When afebrile, there was a mild threshold elevation for all frequencies in the 15-yr-old and a mild elevation of thresholds for just low frequencies in the two siblings. Speech comprehension in quiet was normal but impaired in noise. One of the siblings tested when febrile had a profound elevation (>80 dB) of pure-tone thresholds and speech comprehension was absent. Acoustic reflexes subserving middle ear muscles and olivocochlear bundle were absent when febrile and when afebrile. No other peripheral or cranial nerve abnormalities were found in any of the children. Sensory nerve action potentials from median nerve in one of the children showed no abnormalities on warming of the hand to 39 degrees C.

CONCLUSION

These children have an auditory neuropathy manifested by a disorder of auditory nerve function in the presence of normal cochlear outer hair cell functions. They develop a conduction block of the auditory nerves when their core body temperature rises due, most likely, to a demyelinating disorder of the auditory nerve. The auditory neuropathy in the two affected siblings is likely to be inherited as a recessive disorder.

摘要

目的

明确三名儿童(两名3岁和6岁的兄弟姐妹以及一名15岁的非亲属儿童)发热时出现短暂性耳聋的机制。

设计

采用听力测试(纯音听力测定、言语和句子理解测试)、鼓室导抗图、中耳肌肉反射阈值、耳声发射(OAE)以及电生理方法(听觉脑干反应[ABR]、感觉诱发电位、周围神经传导速度)对儿童在体温正常和发热时进行检测。

结果

体温正常时,ABR异常,IV-V波明显延迟,I-III波缺失。其中一名儿童发热时检测的ABR未显示出ABR成分。使用OAE评估的耳蜗受体功能在发热和体温正常状态下均正常。三名儿童均存在耳蜗微音器电位,两名儿童可能存在总和电位。体温正常时,15岁儿童所有频率的阈值有轻度升高,两名兄弟姐妹仅低频阈值有轻度升高。安静环境下的言语理解正常,但在噪声环境中受损。一名发热时接受测试的兄弟姐妹纯音阈值显著升高(>80 dB),且无言语理解能力。发热和体温正常时,中耳肌肉和橄榄耳蜗束的声反射均缺失。所有儿童均未发现其他周围或颅神经异常。一名儿童手部加热至39摄氏度时,正中神经的感觉神经动作电位未显示异常。

结论

这些儿童存在听觉神经病,表现为耳蜗外毛细胞功能正常但听觉神经功能障碍。他们在核心体温升高时出现听觉神经传导阻滞,很可能是由于听觉神经脱髓鞘疾病所致。两名受影响的兄弟姐妹中的听觉神经病可能以隐性疾病形式遗传。

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