• 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

小眼球后部的超声生物显微镜检查和光学相干断层扫描结果

Ultrasound biomicroscopy and OCT findings in posterior microphthalmos.

作者信息

Erdol H, Kola M, Turk A, Akyol N

机构信息

Department of Ophthalmology, Karadeniz Technical University, School of Medicine, Trabzon - Turkey.

出版信息

Eur J Ophthalmol. 2008 May-Jun;18(3):479-82. doi: 10.1177/112067210801800331.

DOI:10.1177/112067210801800331
PMID:18465740
Abstract

PURPOSE

Posterior microphthalmos is a rare ocular abnormality. The authors report two siblings with bilateral posterior microphthalmos.

METHODS

Two siblings (aged 10 and 13) were admitted with a history of low degree of vision. Ophthalmologic examinations, ocular ultrasonography, ultrasonic biomicroscopy (UBM), and optical coherence tomography (OCT) investigations were carried out and the results were evaluated. All results were also compared with their normal sibling.

RESULTS

Two siblings with posterior microphthalmos have normal and near normal anterior segment dimensions, shortened axial lengths (smaller than 17 mm), low vision with high hyperopias, papillomacular folds, and crowded optic discs. OCT investigation showed bilateral papillomacular retinal fold and UBM examination showed that ciliary body moved behind the iris towards the pupilla and the iridocorneal angle anomalies in two siblings. These findings were not observed in the normal sibling.

CONCLUSIONS

Posterior microphthalmos can exist in the presence of some ocular anomalies. In this case report, UBM provided new information about the structure of iridocorneal angle and ciliary body.

摘要

目的

后部小眼球是一种罕见的眼部异常。作者报告了两名患有双侧后部小眼球的兄弟姐妹。

方法

两名兄弟姐妹(年龄分别为10岁和13岁)因视力低下病史入院。进行了眼科检查、眼部超声检查、超声生物显微镜检查(UBM)和光学相干断层扫描(OCT)检查,并对结果进行了评估。所有结果还与他们正常的兄弟姐妹进行了比较。

结果

两名患有后部小眼球的兄弟姐妹前节尺寸正常或接近正常,眼轴长度缩短(小于17毫米),高度远视导致视力低下,存在视乳头黄斑皱褶和拥挤的视盘。OCT检查显示双侧视乳头黄斑视网膜皱褶,UBM检查显示两名兄弟姐妹的睫状体向瞳孔方向移至虹膜后方且存在虹膜角膜角异常。这些发现在正常的兄弟姐妹中未观察到。

结论

后部小眼球可能伴有一些眼部异常。在本病例报告中,UBM提供了有关虹膜角膜角和睫状体结构的新信息。

相似文献

1
Ultrasound biomicroscopy and OCT findings in posterior microphthalmos.小眼球后部的超声生物显微镜检查和光学相干断层扫描结果
Eur J Ophthalmol. 2008 May-Jun;18(3):479-82. doi: 10.1177/112067210801800331.
2
Pervasive ocular anomalies in posterior microphthalmos.后部小眼球中的普遍性眼部异常。
Optometry. 2007 Feb;78(2):71-7. doi: 10.1016/j.optm.2006.08.016.
3
Clinical features of posterior microphthalmos associated with papillomacular fold and high hyperopia.伴有黄斑乳头皱褶和高度远视的后部小眼球的临床特征。
Clin Exp Optom. 2016 Nov;99(6):590-593. doi: 10.1111/cxo.12371. Epub 2016 May 10.
4
Posterior segment changes associated with posterior microphthalmos.与后部小眼球相关的后段改变。
Ophthalmology. 2002 Mar;109(3):569-74. doi: 10.1016/s0161-6420(01)00996-4.
5
Detailed ophthalmologic evaluation of posterior microphthalmos.小眼球后部的详细眼科评估。
Middle East Afr J Ophthalmol. 2014 Apr-Jun;21(2):186-8. doi: 10.4103/0974-9233.129774.
6
Optical coherence tomography of bilateral posterior microphthalmos with papillomacular fold and novel features of retinoschisis and dialysis.双侧小眼球合并视乳头黄斑皱褶的光学相干断层扫描及视网膜劈裂和视网膜脱离的新特征
Am J Ophthalmol. 2004 Sep;138(3):480-1. doi: 10.1016/j.ajo.2004.03.015.
7
Spectral domain optical coherence tomography findings in retinal folds associated with posterior microphthalmos.与后部小眼球相关的视网膜褶皱的频域光学相干断层扫描结果
J AAPOS. 2012 Aug;16(4):389-91. doi: 10.1016/j.jaapos.2012.02.020. Epub 2012 Jul 25.
8
CLINICAL APPRAISAL AND RETINAL IMAGING IN POSTERIOR MICROPHTHALMOS.后段小眼球的临床评估与视网膜成像
Semin Ophthalmol. 2018;33(3):412-418. doi: 10.1080/08820538.2017.1284869. Epub 2017 Feb 15.
9
The posterior pole and papillomacular fold in posterior microphthalmos: novel spectral-domain optical coherence tomography findings.后部小眼畸形的后极和乳头黄斑皱褶:新型频域光相干断层扫描发现。
Ophthalmology. 2013 Aug;120(8):1656-64. doi: 10.1016/j.ophtha.2013.01.026. Epub 2013 May 19.
10
Bilateral microphthalmos with poor visual acuity, high hyperopia, and papillomacular retinal folds in siblings.兄弟姐妹中出现双眼小眼球,伴有视力差、高度远视和视网膜乳头黄斑皱褶。
Jpn J Ophthalmol. 1995;39(2):177-9.

引用本文的文献

1
Multimodal imaging in posterior microphthalmos.小眼球后部的多模态成像
J Curr Ophthalmol. 2019 Feb 4;31(3):335-338. doi: 10.1016/j.joco.2019.01.001. eCollection 2019 Sep.
2
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3.新发现的 MYRF 基因截断突变导致常染色体显性遗传的高度远视,定位于 11p12-q13.3。
Hum Genet. 2019 Oct;138(10):1077-1090. doi: 10.1007/s00439-019-02039-z. Epub 2019 Jun 6.
3
Detailed ophthalmologic evaluation of posterior microphthalmos.小眼球后部的详细眼科评估。
Middle East Afr J Ophthalmol. 2014 Apr-Jun;21(2):186-8. doi: 10.4103/0974-9233.129774.
4
Autosomal-recessive posterior microphthalmos is caused by mutations in PRSS56, a gene encoding a trypsin-like serine protease.常染色体隐性遗传型后部小眼症由 PRSS56 基因突变引起,该基因编码一种胰蛋白酶样丝氨酸蛋白酶。
Am J Hum Genet. 2011 Mar 11;88(3):382-90. doi: 10.1016/j.ajhg.2011.02.006.