• 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

黏多糖贮积症 I 型(Hurler 综合征)患儿眼轴长度和角膜屈光度。

Ocular axial length and corneal refraction in children with mucopolysaccharidosis (MPS I-Hurler).

机构信息

Department of Clinical Neuroscience, Karolinska Institutet, St. Erik Eye Hospital, Sweden.

出版信息

Acta Ophthalmol. 2012 May;90(3):287-90. doi: 10.1111/j.1755-3768.2010.01934.x. Epub 2010 Jun 10.

DOI:10.1111/j.1755-3768.2010.01934.x
PMID:20553232
Abstract

BACKGROUND/AIMS: To assess corneal refraction and axial length in children with mucopolysaccharidosis I-Hurler (MPS I-H), treated early with stem cell transplantation (SCT), in order to establish possible causes of hyperopia.

METHODS

Clinical ophthalmological follow-up included keratometry and measurements of axial length.

RESULTS

Five patients, with SCT performed before 23 months of age, were examined. Median age was 8.2 years (range 5.2-10.5). Best-corrected decimal visual acuity was ≥ 0.5 (≥ 20/40 Snellen fraction) in seven of 10 eyes. High hyperopia, ranging from +4.0 to +9.0 spherical equivalents, was noted in all 10 eyes. Mild to moderate corneal opacities occurred in all 10 eyes. Optic disc areas, borders and cuppings were normal in all 10 eyes. No patient had glaucoma. Keratometry could be performed in five patients and demonstrated low values in the group ranging from 38.24 to 41.56 Diopters (D) right eye to 38.24-41.94 D left eye, which was significantly lower than the age matching reference material (p < 0.05). Axial lengths, available in five patients, ranged between 20.68 to 21.57 mm right eye and 20.52 to 21.38 mm left eye, which also was lower than the age matching reference material (p < 0.05).

CONCLUSION

Reduced axial length together with reduced corneal refraction is suggested to be causative to the hyperopia in patients with MPS I Hurler. Detection of refractive errors and prescription of eye glasses are important to avoid amblyopia.

摘要

背景/目的:评估接受早期干细胞移植(SCT)治疗的黏多糖贮积症 I-Hurler 型(MPS I-H)患儿的角膜屈光度和眼轴长度,以确定远视的可能原因。

方法

临床眼科随访包括角膜曲率计和眼轴长度测量。

结果

5 名患者在 23 个月龄前接受 SCT 治疗,中位年龄为 8.2 岁(5.2-10.5 岁)。10 只眼中有 7 只的最佳矫正十进制视力≥0.5(≥20/40 斯涅伦分数)。10 只眼中均出现高度远视,范围为+4.0 至+9.0 球镜等效。10 只眼中均出现轻度至中度角膜混浊。10 只眼中的视盘面积、边界和凹陷均正常。无一例患者患有青光眼。5 名患者可进行角膜曲率计检查,结果显示该组右眼范围为 38.24 至 41.56 屈光度(D),左眼为 38.24 至 41.94 D,明显低于年龄匹配的参考值(p<0.05)。5 名患者的眼轴长度范围为右眼 20.68 至 21.57mm,左眼 20.52 至 21.38mm,也低于年龄匹配的参考值(p<0.05)。

结论

轴长缩短和角膜屈光度降低被认为是 MPS I-H 患者远视的原因。检测屈光不正并配镜对于避免弱视非常重要。

相似文献

1
Ocular axial length and corneal refraction in children with mucopolysaccharidosis (MPS I-Hurler).黏多糖贮积症 I 型(Hurler 综合征)患儿眼轴长度和角膜屈光度。
Acta Ophthalmol. 2012 May;90(3):287-90. doi: 10.1111/j.1755-3768.2010.01934.x. Epub 2010 Jun 10.
2
Corneal hysteresis in mucopolysaccharidosis I and VI.黏多糖贮积症 I 型和 VI 型的角膜滞后性。
Acta Ophthalmol. 2012 Aug;90(5):445-8. doi: 10.1111/j.1755-3768.2010.02085.x. Epub 2011 Jan 14.
3
Ocular findings in four children with mucopolysaccharidosis I-Hurler (MPS I-H) treated early with haematopoietic stem cell transplantation.4例黏多糖贮积症I型(Hurler综合征,MPS I-H)患儿早期接受造血干细胞移植后的眼部表现
Acta Ophthalmol Scand. 2006 Dec;84(6):781-5. doi: 10.1111/j.1600-0420.2006.00743.x.
4
Axial Lengths in Children with Recessive Cornea Plana.隐性扁平角膜患儿的眼轴长度
Ophthalmic Genet. 2015 Jun;36(2):123-5. doi: 10.3109/13816810.2013.851249. Epub 2013 Dec 4.
5
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.
6
Laser-assisted subepithelial keratectomy for bilateral hyperopia and hyperopic anisometropic amblyopia in children: one-year outcomes.激光辅助下的上皮下角膜切除术治疗儿童双侧远视和远视性屈光参差性弱视:一年随访结果。
J Cataract Refract Surg. 2010 Feb;36(2):260-7. doi: 10.1016/j.jcrs.2009.08.022.
7
Excimer laser photorefractive keratectomy for hyperopia: 7.5-year follow-up.准分子激光光折射性角膜切削术治疗远视:7.5 年随访。
J Cataract Refract Surg. 2005 Jun;31(6):1104-13. doi: 10.1016/j.jcrs.2004.10.051.
8
Biometric and molecular characterization of clinically diagnosed posterior microphthalmos.临床诊断的后小眼球症的生物特征和分子特征。
Am J Ophthalmol. 2013 Feb;155(2):361-372.e7. doi: 10.1016/j.ajo.2012.08.016. Epub 2012 Nov 3.
9
Photorefractive keratectomy for pediatric anisometropia: safety and impact on refractive error, visual acuity, and stereopsis.儿童屈光参差性屈光性角膜切削术:安全性及其对屈光不正、视力和立体视的影响
Am J Ophthalmol. 2004 Jul;138(1):70-8. doi: 10.1016/j.ajo.2004.01.044.
10
Longitudinal Changes in Refractive Development in Highly Hyperopic Children: A 2.6-11.2 Year Follow-up of Preschoolers Diagnosed with High Hyperopia.高度远视儿童的屈光发育纵向变化:对被诊断为高度远视的学龄前儿童进行的 2.6-11.2 年随访。
Curr Eye Res. 2024 Jul;49(7):768-775. doi: 10.1080/02713683.2024.2336162. Epub 2024 Apr 14.

引用本文的文献

1
Objectively measuring anterior segment alterations in the eyes of mucopolysaccharidoses: Its utility in early diagnosis of glaucoma.客观测量黏多糖贮积症患者眼前节改变:对青光眼早期诊断的应用价值。
Indian J Ophthalmol. 2022 Dec;70(12):4180-4185. doi: 10.4103/ijo.IJO_1300_22.
2
Mucopolysaccharidosis: A broad review.黏多糖贮积症:全面综述。
Indian J Ophthalmol. 2022 Jul;70(7):2249-2261. doi: 10.4103/ijo.IJO_425_22.
3
Anterior segment optical coherence tomography and in vivo confocal microscopy in cases of mucopolysaccharidosis.
黏多糖贮积症病例中的眼前节光学相干断层扫描和活体共聚焦显微镜检查
Am J Ophthalmol Case Rep. 2020 Apr 30;19:100728. doi: 10.1016/j.ajoc.2020.100728. eCollection 2020 Sep.
4
Ophthalmological Findings in Mucopolysaccharidoses.黏多糖贮积症的眼科表现
J Clin Med. 2019 Sep 14;8(9):1467. doi: 10.3390/jcm8091467.
5
Ophthalmologic manifestations in Taiwanese patients with mucopolysaccharidoses.台湾黏多糖贮积症患者的眼科表现
Mol Genet Genomic Med. 2019 May;7(5):e00617. doi: 10.1002/mgg3.617. Epub 2019 Mar 8.
6
Ocular features in mucopolysaccharidosis: diagnosis and treatment.黏多糖贮积症的眼部特征:诊断与治疗。
Ital J Pediatr. 2018 Nov 16;44(Suppl 2):125. doi: 10.1186/s13052-018-0559-9.
7
Ocular manifestations and management recommendations of lysosomal storage disorders I: mucopolysaccharidoses.溶酶体贮积症的眼部表现及管理建议I:黏多糖贮积症
Clin Ophthalmol. 2015 Sep 7;9:1633-44. doi: 10.2147/OPTH.S78368. eCollection 2015.
8
Spectral domain optical coherence tomography imaging of mucopolysaccharidoses I, II, and VI A.黏多糖贮积症 I 型、II 型和 VI A 型的光谱域光学相干断层扫描成像
Graefes Arch Clin Exp Ophthalmol. 2015 Dec;253(12):2111-9. doi: 10.1007/s00417-015-2953-y. Epub 2015 Feb 18.
9
Enzyme replacement therapy for Mucopolysaccharidosis Type I among patients followed within the MPS Brazil Network.MPS 巴西网络中接受治疗的黏多糖贮积症 I 型患者的酶替代疗法。
Genet Mol Biol. 2014 Mar;37(1):23-9. doi: 10.1590/s1415-47572014000100006. Epub 2013 Feb 28.
10
Clinical overview and treatment options for non-skeletal manifestations of mucopolysaccharidosis type IVA.黏多糖贮积症 IVA 型非骨骼表现的临床概述和治疗选择。
J Inherit Metab Dis. 2013 Mar;36(2):309-22. doi: 10.1007/s10545-012-9459-0. Epub 2012 Feb 23.