Suppr超能文献

遗传性先天性单侧耳聋:一种新疾病?

Hereditary congenital unilateral deafness: a new disorder?

作者信息

Dikkers Frederik G, Verheij Joke B G M, van Mechelen Monique

机构信息

Department of Otorhinolaryngology, University Medical Center Groningen, PO Box 30.001, 9700 RB Groningen, The Netherlands.

出版信息

Ann Otol Rhinol Laryngol. 2005 Apr;114(4):332-7. doi: 10.1177/000348940511400414.

Abstract

Congenital unilateral deafness is a rare disorder. The prevalence rates are unknown. The prevalence of children with severe to profound hearing losses that are congenital (or acquired before the development of speech and language) is 0.5 to 3 per 1,000 live births. Evidently, congenital unilateral deafness must have a lower prevalence. The purpose of this research was to present a new disorder, hereditary congenital unilateral deafness. A pedigree is presented in which both male and female members display symptoms of congenital unilateral deafness. Two affected persons and a normal-hearing member of the family have vestibular abnormalities without dysequilibrium. The inheritance pattern of this new syndrome is not clear. We hypothesize that the disorder might be new. A family like this has never before been presented in the medical literature.

摘要

先天性单侧耳聋是一种罕见的疾病。其患病率未知。先天性(或在言语和语言发育之前获得性)重度至极重度听力损失儿童的患病率为每1000例活产中有0.5至3例。显然,先天性单侧耳聋的患病率肯定更低。本研究的目的是提出一种新的疾病——遗传性先天性单侧耳聋。现展示一个家系,其中男性和女性成员均表现出先天性单侧耳聋的症状。该家族中有两名患者和一名听力正常的成员存在前庭异常但无平衡失调。这种新综合征的遗传模式尚不清楚。我们推测这种疾病可能是新出现的。医学文献中此前从未报道过这样的家族。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验