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(What’s the story) morning glory? MRI findings in morning glory disc anomaly
NeuroradiologyMorning glory disc anomaly (MGDA) is a rare congenital ophthalmologic disorder. Historically it has been diagnosed fundoscopically, with little in the literature regarding its imaging findings. The purpose of this study is to further characterize the orbital and associated intracranial magnetic resonance imaging (MRI) findings of MGDA in our tertiary ...
Caoilfhionn Ní Leidhin +11 more
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Morning Glory Disc Anomaly or Optic Disc Coloboma?
Archives of Ophthalmology, 1994I read with interest the case report by Dailey and colleagues 1 in the April 1993 issue of theArchives. The morphologic features of the optic nerve abnormality that they have superbly photographed are compatible with the so-called morning glory anomaly. The dysplasia in this patient is on the mild end of the spectrum 2 and vision is well preserved. The
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Morning Glory Disc Anomaly in an Infant
Journal of Pediatric Ophthalmology & Strabismus, 2023Erlend C S, Landsend +2 more
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The Morning Glory Disc Anomaly: Contractile Movement, Classification, and Embryogenesis
Documenta Ophthalmologica, 1987A case of the morning glory disc anomaly is reported in which alternating contraction and dilation movements were observed and documented with fundus photographs. The movements are attributed to an anomalous communication between the subretinal and subarachnoid spaces that permits flux of fluid to occur between the two compartments, with consequent ...
exaly +3 more sources
The Spectrum in the Morphology of the So-Called "Morning Glory Disc Anomaly"
Journal of Pediatric Ophthalmology & Strabismus, 1988ABSTRACT Eight cases illustrating the different configurations of the morning glory disc anomaly are presented. The spectrum of the appearance is due to variability in excavation of the disc, amount of glial tissue and hyaloid system remnants in the center of the disc, and degree of peripapillary pigmentary changes.
E I, Traboulsi, J F, O'Neill
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Reversible Carotid Artery Narrowing in Morning Glory Disc Anomaly
Journal of Neuro-Ophthalmology, 2005A 14-year-old boy with morning glory disc anomaly (MGDA) and normal visual and neurologic function displayed marked carotid artery narrowing on magnetic resonance angiography (MRA). This narrowing disappeared on a follow-up MRA six months later. Optic coherence tomography and scanning laser polarimetry disclosed a normal retinal nerve fiber layer in ...
Marjorie A, Murphy +5 more
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Morning Glory Disc Anomaly With Chiari Type I Malformation
Journal of Pediatric Ophthalmology & Strabismus, 2014Morning glory disc anomaly is a rare optic nerve dysplasia associated with various neovascular abnormalities. Due to these associations, children with morning glory disc anomaly have brain imaging and angiography to detect other congenital defects.
Tim, Arlow +3 more
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Persistence of the Primary Vitreous in Association with the Morning Glory Disc Anomaly
Journal of Pediatric Ophthalmology & Strabismus, 1984ABSTRACT Two patients with the morning glory disc anomaly are reported. In one, fibrovascular stalk passed forward into the vitreous cavity, while in the second a persistent hyaloid artery extended anteriorly from a tuft of fibrous tissue to the posterior lens capsule.
G C, Brown, J, Gonder, A, Levin
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Optical coherence tomographic characteristics in morning glory disc anomaly
Canadian Journal of Ophthalmology, 2007Optical coherence tomography (OCT) confirms increased optic nerve head dimensions in morning glory anomaly, and provides evidence of increased retinal nerve fibre layer thickness and reduced macular thickness.This first report of quantitative data from OCT may provide more useful information to corroborate clinical diagnosis of this rare congenital ...
Geetha, Srinivasan +2 more
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Unilateral Morning Glory Disc Anomaly With Ipsilateral Limbal Dermoids
Journal of Pediatric Ophthalmology & Strabismus, 2014The authors present the case of a child with multiple limbal dermoids and morning glory disc anomaly in the right eye. These anomalies are rarely associated and this is the first report of co-occurrence in the same eye in a patient without additional systemic anomalies. [J Pediatr Ophthalmol Strabismus 2014;51:e37–e39.]
Eugene A, Lowry +1 more
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