• 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

An uncommon cause of vision loss: Leber hereditary optic neuropathy.

作者信息

Glover Julie M, Casmaer Monica L, April Michael D

机构信息

Julie M. Glover practices emergency medicine at Wright Patterson Medical Center at Wright Patterson Air Force Base in Dayton, Ohio, and is an adjunct professor in the PA program at Kettering (Ohio) College. Monica L. Casmaer is program director at Brooke Army Medical Center in San Antonio, Tex., and a faculty member of the US Army/Baylor University doctor of science emergency medicine physician assistant program in Dallas, Tex. Michael D. April is assistant program director for research in the emergency medicine residency at the San Antonio Uniformed Services Health Education Consortium. The views expressed in this article are those of the authors and do not reflect the official policy or position of Brooke Army Medical Center, the US Army Medical Department, the US Army Office of the Surgeon General, the Department of the Army, the Department of the Air Force and Department of Defense or the US government. The authors have disclosed no potential conflicts of interest, financial or otherwise.

出版信息

JAAPA. 2018 Nov;31(11):32-34. doi: 10.1097/01.JAA.0000546478.56818.50.

DOI:10.1097/01.JAA.0000546478.56818.50
PMID:30358677
Abstract

Leber hereditary optic neuropathy (LHON) is a rare mitochondrial genetic disorder characterized by painless acute or subacute vision loss that develops during adolescence. Clinicians should know how to identify potential LHON and when to refer patients to a neuro-ophthalmologist for diagnosis and treatment. This case highlights the value of a thorough family history in ED patients.

摘要

相似文献

1
An uncommon cause of vision loss: Leber hereditary optic neuropathy.
JAAPA. 2018 Nov;31(11):32-34. doi: 10.1097/01.JAA.0000546478.56818.50.
2
Late-onset Leber hereditary optic neuropathy.迟发性莱伯遗传性视神经病变。
Clin Exp Ophthalmol. 2013 Sep-Oct;41(7):690-3. doi: 10.1111/ceo.12091. Epub 2013 Apr 11.
3
[Recurrent visual loss in Leber hereditary optic neuropathy: a case report].[Leber遗传性视神经病变中的复发性视力丧失:一例报告]
J Fr Ophtalmol. 2008 Apr;31(4):409-15. doi: 10.1016/s0181-5512(08)71436-0.
4
Clinical and electrophysiology findings in Slovene patients with Leber hereditary optic neuropathy.斯洛文尼亚莱伯遗传性视神经病变患者的临床及电生理检查结果
Doc Ophthalmol. 2015 Jun;130(3):179-87. doi: 10.1007/s10633-015-9489-7. Epub 2015 Feb 19.
5
Recurrent visual loss in Leber hereditary optic neuropathy.
Arch Ophthalmol. 2003 Feb;121(2):288-91. doi: 10.1001/archopht.121.2.288.
6
Severe sequential visual loss in MS co-diagnosis of Leber's hereditary optic neuropathy.多发性硬化症合并Leber遗传性视神经病变时的严重连续性视力丧失。
Can J Ophthalmol. 2019 Apr;54(2):e69-e70. doi: 10.1016/j.jcjo.2018.06.020. Epub 2018 Aug 30.
7
[A teenager with acute bilateral visual loss].[一名患有急性双侧视力丧失的青少年]
Tidsskr Nor Laegeforen. 2018 Aug 10;138(12). doi: 10.4045/tidsskr.17.0802. Print 2018 Aug 21.
8
Painful vision loss in Leber hereditary optic neuropathy with novel ND1 variant mimicking optic neuritis.
Can J Ophthalmol. 2023 Feb;58(1):e40-e42. doi: 10.1016/j.jcjo.2022.06.007. Epub 2022 Jul 6.
9
[Leber's hereditary optic neuropathy].[莱伯遗传性视神经病变]
Ophthalmologe. 2011 Dec;108(12):1179-92; quiz 1193-4. doi: 10.1007/s00347-011-2482-y.
10
Natural History of Conversion of Leber's Hereditary Optic Neuropathy: A Prospective Case Series.Leber 遗传性视神经病变的自然病程:一项前瞻性病例系列研究。
Ophthalmology. 2017 Jun;124(6):843-850. doi: 10.1016/j.ophtha.2017.01.002. Epub 2017 Feb 10.