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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; Elham Soltani MD; Omid Fakhrizadeh MD
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Presentation Type:
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Oral
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Subject:
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Posterior Segment
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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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Al-Zahra Eye Center, Zahedan University of Medical Sciences, Zahedan, Iran
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E mail:
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mojtaba_abrishami@yahoo.com
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Phone:
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05118433192
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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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An eighteen years old young man was referred with high hyperopia for refractive surgery. 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 17.89 mm and 18.14 mm in LE. Except a shallow anterior chamber, anterior segment was normal. In fundus exam, a papillomacular retinal fold extending from the center of the fovea 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, steep cornea and thick Papillomacular fold with a relative good vision.
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Attachment:
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