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مقاله
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Abstract
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Title:
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Bilateral Posterior Microphthalmos Associated with Papillomacular Fold, Severe Hyperopia and Steep Cornea
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Author(s):
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Mojtaba Abrishami MD; Alireza Maleki MD; Ali Hamidian-Shoormasti MD
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Presentation Type:
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Poster
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Subject:
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Posterior Segment and Uveitis
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Others:
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Presenting Author:
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Name:
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Mojtaba Abrishami
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Affiliation :(optional)
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Eye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, Iran
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E mail:
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mojtaba_abrishami@yahoo.com
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Phone:
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02166481649
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Mobile:
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09155207987
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Purpose:
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To report a young patient with microphthalmos associated with bilateral papillomacular fold and severe hyperopia.
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Methods:
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Observational case report
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Results:
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A sixteen years old young man was referred with high hyperopia for checkup. Spherical error in right eye (RE) was +14.75D and in the left eye (LE) was +15.00D without astigmatism. Keratometry was reported 51.50,52.25@113 in RE and 51.25,52.25@65 in LE Best corrected visual acuity was 20/25 in both eyes. Axial length in RE was 14.8 mm and 14.9 mm in LE. Also cornea diameter measured 9.9 for both eyes. In fundus exam, a papillomacular retinal fold extending from the center of thefovea toward the optic nerve head was present. In OCT exam, papillomacular fold with thickness of 322 microns in RE and 277 microns in LE were reported. In Pentacam exam, anterior chamber depth, central corneal thickness and anterior and posterior BFS were reported 2.34mm, 565microns, 6.54mm and 5.39mm in RE and 2.41mm, 578microns, 6.54mm and 5.39mm in LE. Intraocular pressure was 13 mmHg in both eyes and there was no sign of angle closure glaucoma.
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Conclusion:
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Microphthalmos may be associated with high hypermetropia, thick papillomacular fold,and steep cornea with a relative good vision.
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Attachment:
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5912.pptx
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