Case report: Meniere's disease and otosclerosis - Different outcomes of the same disease?

被引:5
作者
Klockars, Tuomas
Kentala, Ema
机构
[1] Kymenlaakso Cent Hosp, Dept Otorhinolaryngol, Kotka 48210, Finland
[2] Univ Helsinki, Cent Hosp, Dept Otorhinolaryngol, Helsinki 00029, Finland
关键词
Meniere's disease; otosclerosis; inheritance; genetics;
D O I
10.1016/j.anl.2006.09.020
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
The etiologies of Meniere's disease and otosclerosis are largely unknown. An association between these two diseases has been proposed on both a clinical and histopathologic basis but the causal relationship is controversial. In this paper we report two families in which both otosclerosis and Meniere's disease are inherited as independent phenotypes suggesting that the two diseases represent different outcomes of the same mutation. Thus the Meniere's disease occasionally seen in otosclerotic patients might not be caused by otosclerosis, but rather by a molecular defect leading to endolymphatic hydrops and/or clinical otosclerosis. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:101 / 104
页数:4
相关论文
共 7 条
  • [1] OTOSCLEROSIS - VESTIBULAR SYMPTOMS AND SENSORINEURAL HEARING-LOSS
    CODY, DTR
    BAKER, HL
    [J]. ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1978, 87 (06) : 778 - 796
  • [2] FRANKLIN DJ, 1990, AM J OTOL, V11, P135
  • [3] The aetiology of otosclerosis: a review of the literature
    Menger, DJ
    Tange, RA
    [J]. CLINICAL OTOLARYNGOLOGY, 2003, 28 (02) : 112 - 120
  • [4] Meniere's disease
    Minor, LB
    Schessel, DA
    Carey, JP
    [J]. CURRENT OPINION IN NEUROLOGY, 2004, 17 (01) : 9 - 16
  • [5] Genetics (molecular biology) and Meniere's disease
    Morrison, AW
    Johnson, KJ
    [J]. OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA, 2002, 35 (03) : 497 - +
  • [6] Etiopathogenesis of otosclerosis
    Niedermeyer, HP
    Arnold, W
    [J]. ORL-JOURNAL FOR OTO-RHINO-LARYNGOLOGY AND ITS RELATED SPECIALTIES, 2002, 64 (02): : 114 - 119
  • [7] Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
    Robertson, NG
    Lu, L
    Heller, S
    Merchant, SN
    Eavey, RD
    McKenna, M
    Nadol, JB
    Miyamoto, RT
    Linthicum, FH
    Neto, JFL
    Hudspeth, AJ
    Seidman, CE
    Morton, CC
    Seidman, JG
    [J]. NATURE GENETICS, 1998, 20 (03) : 299 - 303