• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Heredity hearing losses with delayed onset: mechanisms of expression.

作者信息

Jahn A F, Noyek A M

出版信息

Otolaryngol Clin North Am. 1981 Feb;14(1):59-64.

PMID:6789283
Abstract

Inherited hearing loss with a delayed onset is a feature of an intriguing group of disorders. The mechanisms whereby delayed hearing loss develops may be grouped as primary degenerative (abiotrophic) disorders, secondary degenerative disorders, dysgenerative disorders, and disorders of inappropriate response. Illustrative examples within these four groups are discussed. The difficulties in determining the preclinical latent state in inherited disorders are briefly outlined.

摘要

相似文献

1
Heredity hearing losses with delayed onset: mechanisms of expression.
Otolaryngol Clin North Am. 1981 Feb;14(1):59-64.
2
Hearing loss is a common feature of symptomatic children with profound biotinidase deficiency.听力损失是有严重生物素酶缺乏症的有症状儿童的一个常见特征。
J Pediatr. 2002 Feb;140(2):242-6. doi: 10.1067/mpd.2002.121938.
3
[Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children].[现代关于遗传在儿童单症状听力障碍起源中作用的概念]
Vestn Otorinolaringol. 1980 Jan-Feb(1):67-73.
4
Hearing loss associated with hereditary diseases and syndromes.与遗传性疾病和综合征相关的听力损失。
Ear Nose Throat J. 1983 Nov;62(11):571-93.
5
Hearing loss.听力损失
J Fam Pract. 1981 Jun;12(6):1053-8.
6
[Genetic sensorineural hearing loss in childhood].[儿童遗传性感音神经性听力损失]
Kulak Burun Bogaz Ihtis Derg. 2002 Mar-Apr;9(2):99-105.
7
[Otosclerotic syndromes with hereditary disorders of collagen].[伴有遗传性胶原蛋白疾病的耳硬化综合征]
Cesk Otolaryngol. 1971 Feb;20(1):3-6.
8
[Late hereditary degenerative sensorineural hearing loss associated with IgA mesangial glomerulonephritis of probable autosomal dominant heredity].[与可能为常染色体显性遗传的IgA系膜增生性肾小球肾炎相关的迟发性遗传性退行性感音神经性听力损失]
Acta Otorrinolaringol Esp. 1993 Nov-Dec;44(6):447-54.
9
Hearing, language, speech, vestibular, and dentofacial disorders in fetal alcohol syndrome.胎儿酒精综合征中的听力、语言、言语、前庭及牙面疾病。
Alcohol Clin Exp Res. 1997 Apr;21(2):227-37.
10
Audiological profile in Apert syndrome.Apert综合征的听力学特征
Arch Dis Child. 2005 Jun;90(6):592-3. doi: 10.1136/adc.2004.067298.