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马凡综合征伴双侧晶状体异位及孤立性晶状体缺损

Bilateral ectopia lentis with isolated lens coloboma in Marfan syndrome.

作者信息

Sahu Sabin, Yadav Reena, Gupta Sharad, Raj Puri Lila

机构信息

Sagarmatha Choudhary Eye Hospital, Lahan, Nepal.

出版信息

GMS Ophthalmol Cases. 2016 Dec 5;6:Doc14. doi: 10.3205/oc000051. eCollection 2016.

DOI:10.3205/oc000051
PMID:28028488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5144584/
Abstract

A rare case of bilateral ectopia lentis with isolated lens coloboma in Marfan syndrome is reported. A 21-year-old female presented with decreased vision in both eyes. Her unaided visual acuity was 20/200 and 20/400 in the right and left eye, respectively, improving to 20/40 with -4.5 DS/-3.0 DC x 10° correction in the right eye and 20/80 with -10.0 DS/-6.5 Dc x10° correction in the left eye. On slit lamp examination under mydriasis, both eyes revealed ectopia lentis with lens coloboma and stretched zonules. Fundus examination revealed pigmentary changes at the fovea. On systemic evaluation, she was diagnosed with Marfan syndrome. She was prescribed a refractive correction in form of a contact lens and kept under observation.

摘要

报告了一例马凡综合征伴双侧晶状体异位和孤立性晶状体缺损的罕见病例。一名21岁女性双眼视力下降。她的右眼和左眼裸眼视力分别为20/200和20/400,右眼经-4.5DS/-3.0DC×10°矫正后视力提高到20/40,左眼经-10.0DS/-6.5Dc×10°矫正后视力提高到20/80。散瞳下裂隙灯检查显示双眼晶状体异位伴晶状体缺损和悬韧带拉长。眼底检查发现黄斑区色素改变。经全身评估,她被诊断为马凡综合征。她被处方佩戴隐形眼镜进行屈光矫正并接受观察。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f724/5144584/dd29aed19c61/OC-06-14-g-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f724/5144584/2bebcd3517a4/OC-06-14-g-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f724/5144584/dd29aed19c61/OC-06-14-g-002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f724/5144584/2bebcd3517a4/OC-06-14-g-001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f724/5144584/dd29aed19c61/OC-06-14-g-002.jpg

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引用本文的文献

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Int J Ophthalmol. 2025 Feb 18;18(2):358-361. doi: 10.18240/ijo.2025.02.21. eCollection 2025.
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本文引用的文献

1
Lens coloboma in one eye and ectopia lentis in the other eye of a patient with Marfan syndrome.一名马凡综合征患者一只眼睛有晶状体缺损,另一只眼睛有晶状体异位。
BMJ Case Rep. 2014 Dec 9;2014:bcr2014207112. doi: 10.1136/bcr-2014-207112.
2
The revised Ghent nosology for the Marfan syndrome.修订版马凡综合征根特分类法。
J Med Genet. 2010 Jul;47(7):476-85. doi: 10.1136/jmg.2009.072785.
3
Current concepts of ocular manifestations in Marfan syndrome.马凡综合征眼部表现的当前概念。
Surv Ophthalmol. 2006 Nov-Dec;51(6):561-75. doi: 10.1016/j.survophthal.2006.08.008.
4
Congenital lens coloboma and associated pathologies.先天性晶状体缺损及相关病变。
Doc Ophthalmol. 1993;83(4):313-22. doi: 10.1007/BF01204333.
5
Coloboma of lens.晶状体缺损
Indian J Ophthalmol. 1984 Jan-Feb;32(1):21-2.
6
Bilateral coloboma of lens in Marfan's syndrome.马凡综合征双侧晶状体缺损
Indian J Ophthalmol. 1985 May-Jun;33(3):201-2.