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无听力损害的家族性早发性进行性前庭病

Familial early-onset progressive vestibulopathy without hearing impairment.

作者信息

Brantberg Krister

机构信息

Department of Audiology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Acta Otolaryngol. 2003 Aug;123(6):713-7. doi: 10.1080/00016480310002500.

Abstract

A family with early-onset vestibulopathy is presented. The 34-year-old father had experienced brief attacks of vertigo and currently suffers from unsteadiness and oscillopsia during head movements. His two young sons also experience brief attacks of spontaneous vertigo. In vestibular testing all three subjects showed reduced caloric responses. However, only the father showed reduced otolith function (as reflected by the vestibular-evoked myogenic potentials). Further, all three subjects had walked before the age of 1 year and none of them had had any auditory symptoms. It is suggested that they have familial early-onset progressive vestibulopathy affecting the canals before the otoliths but sparing cochlear function.

摘要

本文报告了一个早发性前庭病家族。34岁的父亲曾经历过短暂的眩晕发作,目前在头部运动时出现不稳和视振荡。他的两个年幼儿子也经历过短暂的自发性眩晕发作。在前庭测试中,所有三名受试者的冷热试验反应均降低。然而,只有父亲的耳石功能降低(以前庭诱发肌源性电位为指标)。此外,所有三名受试者在1岁前就会走路,且均无任何听觉症状。提示他们患有家族性早发性进行性前庭病,该病累及半规管早于耳石,且不累及耳蜗功能。

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