Rare bilateral presentation of morning glory disc anomaly
نویسندگان
چکیده
منابع مشابه
Angio OCT of the Macula and Optic Disk in a Rare Case of Bilateral Morning Glory Disc Anomaly
To report a rare case of bilateral morning glory disc anomaly and to evaluate the Angio OCT characteristics of macula and the optic disk in a case of bilateral morning glory disk anomaly.
متن کاملMorning glory disc anomaly: characteristic MR imaging findings.
SUMMARY Establishing the diagnosis of morning glory disc anomaly is crucial to appropriate patient treatment. Although typically made clinically, the diagnosis is not always straightforward, especially in circumstances where physical examination is limited. The goal of this study was to define the spectrum and frequency of orbital findings in a series of patients with funduscopically-confirmed ...
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Although peripapillary staphyloma and morning glory disc anomaly are rarely encountered, accurate differential diagnosis based on disc appearance is essential because of their similar presentations [1]. However, few cases of contractile peripapillary staphyloma and contractile morning glory disc anomaly have been reported. This study describes a rare case of contractile peripapillary staphyloma...
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To cite: Kumar V, Surve A, Chandra P, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2016216729 DESCRIPTION A 3-year-old girl presented with poor vision OD since birth. The best-corrected visual acuity was counting fingers OD and 20/40 OS with +1D in each eye. Esotropia of 45 prism dioptres (PD) was noted in OD. The anterior segment was unremarkable OU. OS...
متن کاملAn unusual case of congenital unilateral Coats's disease associated with morning glory optic disc anomaly.
We present the case of a 13-year-old girl with a right congenital esotropia who at the age of 6 months presented an anomaly of the optic disc and retinal vessels in the same eye. In the following year she developed Coats's disease, rubeosis iridis, and neovascular glaucoma that led to enucleation. Pathological examination confirmed the clinical diagnosis.
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2016
ISSN: 1757-790X
DOI: 10.1136/bcr-2016-215846