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耳硬化症的系谱分析及听力学调查:一项基于大家庭的研究

Pedigree Analysis and Audiological Investigations of Otosclerosis: An Extended Family Based Study.

作者信息

Rekha Santhanam, Ramalingam Ravi, Parani Madasamy

机构信息

Genomics Laboratory, Department of Genetic Engineering, SRM University, Kattankulathur, Kancheepuram, India.

KKR ENT Hospital and Research Institute, Chennai, India.

出版信息

J Audiol Otol. 2018 Oct;22(4):223-228. doi: 10.7874/jao.2018.00122. Epub 2018 Jun 14.

DOI:10.7874/jao.2018.00122
PMID:29890816
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6233934/
Abstract

BACKGROUND AND OBJECTIVES

To analyse the audiometric profile and the pedigree of a large family with otosclerosis to understand the inheritance pattern and its implication in clinical management of the disease. Subjects and.

METHODS

Pedigree analysis was performed on the basis of family history and audiometric tests. Pure tone audiometry, tympanometry, and acoustic reflexes were evaluated for the family members. Audiometric analysis was also carried out for the individuals who have already underwent corrective surgery at the time of study.

RESULTS

Out of 112 family members, 17 were affected individuals, and 11 of them were surgically confirmed. Hearing loss (HL) started unilaterally and progressed to bilateral form. Otosclerosis was presented in early 20's in the first and second generations but it was delayed to mid-late 30's in the fourth generation. An affected female was diagnosed with otosclerosis during her pregnancy. Though the disease was familial, a mother of four affected offspring in this family did not develop otosclerosis until she died at the age of 84.

CONCLUSIONS

The five-generation family, which was analysed in the present study, exhibited autosomal dominant inheritance of otosclerosis with reduced penetrance. Bilateral HL and pregnancy-aggravated otosclerosis were observed in this family. It was found for the first time that the age of onset of the disease delayed in the successive generations. The current study indicated the importance of detailed pedigree analysis for better clinical management of otosclerosis.

摘要

背景与目的

分析一个患有耳硬化症的大家庭的听力图和家系,以了解其遗传模式及其在该疾病临床管理中的意义。对象与……

方法

基于家族病史和听力测试进行家系分析。对家庭成员进行纯音听力测定、鼓室图和声反射评估。对研究时已接受矫正手术的个体也进行了听力分析。

结果

在112名家庭成员中,17人患病,其中11人经手术确诊。听力损失(HL)始于单侧,后发展为双侧。耳硬化症在第一代和第二代中于20岁出头出现,但在第四代中延迟至30岁中后期。一名患病女性在怀孕期间被诊断出患有耳硬化症。尽管该疾病具有家族性,但这个家庭中四个患病后代的母亲直到84岁去世时才患上耳硬化症。

结论

本研究分析的这个五代家庭显示耳硬化症呈常染色体显性遗传,外显率降低。在这个家庭中观察到双侧HL和妊娠加重型耳硬化症。首次发现该病的发病年龄在连续几代中延迟。当前研究表明详细的家系分析对于耳硬化症更好的临床管理具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad9d/6233934/55e698291714/jao-2018-00122f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad9d/6233934/affe8daf3301/jao-2018-00122f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad9d/6233934/55e698291714/jao-2018-00122f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad9d/6233934/affe8daf3301/jao-2018-00122f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad9d/6233934/55e698291714/jao-2018-00122f2.jpg

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本文引用的文献

1
Clinical and audiological characteristics of 1000Hz audiometric notch patients.
Am J Otolaryngol. 2017 Sep-Oct;38(5):521-525. doi: 10.1016/j.amjoto.2017.03.016. Epub 2017 Apr 1.
2
The pathophysiology of otosclerosis: Review of current research.耳硬化症的病理生理学:当前研究综述
Hear Res. 2015 Dec;330(Pt A):51-6. doi: 10.1016/j.heares.2015.07.014. Epub 2015 Aug 12.
3
Carhart notch 2-kHz bone conduction threshold dip: a nondefinitive predictor of stapes fixation in conductive hearing loss with normal tympanic membrane.卡哈特切迹(2千赫兹骨导阈值下降):鼓膜正常的传导性听力损失中镫骨固定的非确定性预测指标。
Arch Otolaryngol Head Neck Surg. 2011 Mar;137(3):236-40. doi: 10.1001/archoto.2011.14.
4
The etiology of otosclerosis: a combination of genes and environment.耳硬化症的病因:基因与环境的结合。
Laryngoscope. 2010 Jun;120(6):1195-202. doi: 10.1002/lary.20934.
5
The genetics of otosclerosis.耳硬化症的遗传学。
Hear Res. 2010 Jul;266(1-2):70-4. doi: 10.1016/j.heares.2009.07.002. Epub 2009 Jul 14.
6
Genetics of otosclerosis.耳硬化症的遗传学。
Otol Neurotol. 2009 Dec;30(8):1021-32. doi: 10.1097/MAO.0b013e3181a86509.
7
Variations in the "Carhart notch" and overclosure after laser-assisted stapedotomy in otosclerosis.耳硬化症激光镫骨足板成形术后“Carhart 切迹”和过闭现象的变化。
Otol Neurotol. 2009 Dec;30(8):1033-6. doi: 10.1097/MAO.0b013e31818edf00.
8
A review on the genetics of otosclerosis.耳硬化症遗传学综述。
Clin Otolaryngol. 2007 Aug;32(4):239-47. doi: 10.1111/j.1365-2273.2007.01475.x.
9
The genetics of otosclerosis: pedigree studies and linkage analysis.耳硬化症的遗传学:系谱研究与连锁分析
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10
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Adv Otorhinolaryngol. 2007;65:17-24. doi: 10.1159/000098664.