• 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

Sensorineural deafness associated with recessive hypophosphataemic rickets.

作者信息

Weir N

出版信息

J Laryngol Otol. 1977 Aug;91(8):717-22. doi: 10.1017/s0022215100084255.

DOI:10.1017/s0022215100084255
PMID:894124
Abstract

Two pairs of siblings suffering from recessive hypophosphataemic rickets are presented, three members of which have some degree of sensorineural deafness and all of which have bilateral marked narrowing of the internal auditory canals. The biochemical explanation of the condition is discussed.

摘要

相似文献

1
Sensorineural deafness associated with recessive hypophosphataemic rickets.
J Laryngol Otol. 1977 Aug;91(8):717-22. doi: 10.1017/s0022215100084255.
2
Hereditary hypophosphataemic rickets with autosomal recessive inheritance and severe osteosclerosis. A report of two cases.常染色体隐性遗传伴严重骨硬化的遗传性低磷血症性佝偻病。两例报告。
J Bone Joint Surg Br. 1978 Aug;60-B(3):430-4. doi: 10.1302/0301-620X.60B3.681423.
3
The petrous temporal bone and deafness in X-linked hypophosphataemic osteomalacia.X连锁低磷性骨软化症中的岩颞骨与耳聋
Clin Radiol. 1988 Sep;39(5):528-30. doi: 10.1016/s0009-9260(88)80224-1.
4
Recessive hypophosphataemic rickets, and possible aetiology of the 'vitamin D-resistant' syndrome.隐性低磷血症性佝偻病以及“维生素D抵抗”综合征的可能病因。
Arch Dis Child. 1976 May;51(5):360-5. doi: 10.1136/adc.51.5.360.
5
Familial hypophosphatemic rickets showing autosomal dominant inheritance.
Birth Defects Orig Artic Ser. 1971 May;7(6):287-95.
6
Hypophosphataemic rickets.低磷性佝偻病
Lancet. 1990 Jan 20;335(8682):178. doi: 10.1016/0140-6736(90)90058-d.
7
Familial hypophosphataemic rickets affecting a father and his two daughters: a case report.家族性低磷血症性佝偻病累及一位父亲及其两个女儿：病例报告
West Afr J Med. 2010 Jul-Aug;29(4):271-4.
8
Radiologic aspects in differential diagnosis of neural and sensory deafness.神经性和感音性耳聋鉴别诊断中的放射学表现
Ann Otol Rhinol Laryngol. 1974 May-Jun;83(3):286-93. doi: 10.1177/000348947408300302.
9
Spinal-cord compression in untreated adult cases of vitamin-D resistant rickets.未经治疗的成人维生素D抵抗性佝偻病病例中的脊髓压迫
J Bone Joint Surg Am. 1968 Jun;50(4):743-52. doi: 10.2106/00004623-196850040-00010.
10
Hypophosphataemic vitamin D-resistant rickets--a cause of spinal stenosis in adults.低磷性维生素D抵抗性佝偻病——成人椎管狭窄的一个病因
Australas Radiol. 1981 Nov;25(3):264-71. doi: 10.1111/j.1440-1673.1981.tb02259.x.

引用本文的文献

1
Involvement of Dmp1 in the Precise Regulation of Hair Bundle Formation in the Developing Cochlea.Dmp1参与发育中耳蜗毛束形成的精确调控。
Biology (Basel). 2023 Apr 20;12(4):625. doi: 10.3390/biology12040625.
2
Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI).婴儿型全身动脉钙化症（GACI）的听力障碍特征。
Orphanet J Rare Dis. 2022 Jul 19;17(1):273. doi: 10.1186/s13023-022-02410-w.
3
Relation between vitamin D deficiency and benign paroxysmal positional vertigo.维生素 D 缺乏与良性阵发性位置性眩晕的关系。
Sci Rep. 2021 Aug 19;11(1):16855. doi: 10.1038/s41598-021-96445-x.
4
Prevalence of Hearing Disorders among Type 2 Diabetes Mellitus Patients with and without Vitamin D Deficiency.2型糖尿病患者中伴有和不伴有维生素D缺乏的听力障碍患病率
Maedica (Bucur). 2020 Mar;15(1):32-36. doi: 10.26574/maedica.2020.15.1.32.
5
A novel auditory ossicles membrane and the development of conductive hearing loss in Dmp1-null mice.Dmp1 基因缺失小鼠新型听觉听小骨膜和传导性听力损失的发生。
Bone. 2017 Oct;103:39-46. doi: 10.1016/j.bone.2017.06.007. Epub 2017 Jun 8.
6
Ectopic Mineralization and Conductive Hearing Loss in Enpp1asj Mutant Mice, a New Model for Otitis Media and Tympanosclerosis.Enpp1asj突变小鼠的异位矿化与传导性听力损失，一种中耳炎和鼓室硬化症的新模型
PLoS One. 2016 Dec 13;11(12):e0168159. doi: 10.1371/journal.pone.0168159. eCollection 2016.
7
Treatment of ear and bone disease in the Phex mouse mutant with dietary supplementation.通过饮食补充治疗Phex小鼠突变体中的耳部和骨骼疾病。
Am J Otolaryngol. 2017 Jan-Feb;38(1):44-51. doi: 10.1016/j.amjoto.2016.09.014. Epub 2016 Sep 28.
8
A Genetic Murine Model of Endolymphatic Hydrops: The Phex Mouse.内淋巴积水的基因小鼠模型：Phex基因敲除小鼠
Curr Otorhinolaryngol Rep. 2014 Sep;2(3):144-151. doi: 10.1007/s40136-014-0048-7.
9
Therapeutic management of hypophosphatemic rickets from infancy to adulthood.从婴儿期到成年期的低磷血症性佝偻病的治疗管理。
Endocr Connect. 2014 Mar 14;3(1):R13-30. doi: 10.1530/EC-13-0103. Print 2014.
10
Hearing impairment in familial X-linked hypophosphatemic rickets.
Eur J Pediatr. 2004 Oct;163(10):622-3. doi: 10.1007/s00431-004-1504-z.