Angio OCT of the Macula and Optic Disk in a Rare Case of Bilateral Morning Glory Disc Anomaly
نویسندگان
چکیده
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.
منابع مشابه
Patient with Morning Glory syndrome
A 6-year-old patient was referred to our ophthalmology service because of an ocular deviation (esotropia) on the right eye for 3 years. Best-corrected visual acuity in right eye and 20/20 in left eye. According to the Krimsky test, the patient showed 15 prism dioptres esotropia in right eye. No changes were observed in biomicroscopy of both eyes and funduscopy of left eye was normal. An optical...
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BACKGROUND This case is unique because it is the first reported case of Down syndrome with morning glory optic disc anomaly in literature. CASE PRESENTATION A 15-year-old girl with features of Down syndrome presented to the Clinic of Ophthalmology for a regular ophthalmologic examination. Her best corrected visual acuity was 20/50 in the right eye and 20/20 in the left eye. The fundus examina...
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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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MGS is an uncommon congenital optic disc anomaly, which was first described by Kindler [1]. It is characterized by an enlarged funnel-shaped dysplastic disc with glial tissue. The retinal vessels are increased in number, appear to arise from the disc edge and run an abnormally straight course over the peripapillary retina [2,3]. Retinal detachment may occur in about one-third of cases of MGS [4...
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INTRODUCTION Morning glory syndrome (MGS) is a rare congenital optic disc anomaly, first reported in 1970. MGS is a nonprogressive and untreatable condition, which usually occurs as an isolated ocular anomaly, and can be associated with the increased incidence of nonrhegmatogenous retinal detachment, and also with strabismus, afferent pupillary defect, visual field defects, presence of hyaloids...
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