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诺里病的电生理研究。一种伴有听力丧失的X连锁隐性性状。

Electrophysiological study of Norrie's disease. An X-linked recessive trait with hearing loss.

作者信息

Parving A, Elberling C, Warburg M

出版信息

Audiology. 1978 Jul-Aug;17(4):293-8. doi: 10.3109/00206097809101299.

Abstract

3 patients with Norrie's diseas were examined with electrocochleography and brain-stem-evoked responses. The examination revealed a hearing loss of pure cochlear origin with no involvement of the brain stem. The disease is inherited as an X-linked recessive trait only affecting males with unaffected female carriers. The results are thus in agreement with previous investigations of the topical lesion in genetic hearing loss.

摘要

对3例诺里病患者进行了耳蜗电图和脑干诱发电位检查。检查发现为单纯耳蜗起源的听力损失,脑干未受累。该疾病以X连锁隐性性状遗传,仅影响男性,女性携带者不受影响。因此,结果与先前关于遗传性听力损失局部病变的研究一致。

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