Results 121 to 130 of about 14,669 (176)
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Ophthalmic Paediatrics and Genetics, 1985
This paper discusses the characteristic features of 'morning glory' syndrome, observed in 49 patients, described in the literature and in three personal observations. 'Morning glory' syndrome is frequently associated with strabismus (20/49 patients), non-rhegmatogenous retinal detachment (13/56 eyes) or remnants of the hyaloid system (10/56 eyes ...
J J De Laey, A Leys
exaly +3 more sources
This paper discusses the characteristic features of 'morning glory' syndrome, observed in 49 patients, described in the literature and in three personal observations. 'Morning glory' syndrome is frequently associated with strabismus (20/49 patients), non-rhegmatogenous retinal detachment (13/56 eyes) or remnants of the hyaloid system (10/56 eyes ...
J J De Laey, A Leys
exaly +3 more sources
Transient visual loss in morning glory syndrome
Russian Annals of OphthalmologyThe causes of monocular transient visual loss (TVL) are diverse, necessitating a careful approach to diagnosis and differential evaluation of multiple conditions. In rare cases, TVL may occur in association with optic disc anomalies such as morning glory syndrome (MGS), coloboma, or optic disc drusen.
N.L. Sheremet +4 more
openaire +3 more sources
The Morning Glory Syndrome Associated with Sphenoidal Encephalocele
Ophthalmology, 1982A 13-year-old girl was found to have a "morning glory" optic disc anomaly associated with remnants of the primitive hyaloid vasculature, midline cleft lip and palate, agenesis of the corpus callosum, and a sphenoidal encephalocele. The association of these developmental anomalies indicates that the "morning glory" optic disc anomaly may occur as part ...
Steven B Koenig +2 more
exaly +3 more sources
The Morning Glory syndrome associated with sphenoethmoidal encephalocele
Ophthalmic Paediatrics and Genetics, 1990A 10-month-old infant was referred to the ophthalmic department of the Royal Victoria Hospital for assessment. Pregnancy and delivery had been normal. At birth, cleft lip, cleft palate, hypertelorism and a soft tissue mass in the mouth were noted.
M, Hope-Ross, S S, Johnston
exaly +3 more sources
Case report: The morning glory syndrome
Australasian journal of optometry, The, 1990This is a report of a single case of morning glory syndrome. The morning glory syndrome is a rare congenital optic disc anomaly which has received scant attention in the ophthalmologic literature. The aetiology of the disorder remains controversial, although it would appear to be related to an isolated coloboma of the optic nerve.
Algis J Vingrys
exaly +2 more sources
Multimodal imaging of morning glory syndrome with persistent hyperplastic primary vitreous
Journal of Clinical Ultrasound, 2023Morning glory syndrome (MGS) and persistent hyperplastic primary vitreous (PHPV) are congenital abnormity, which may be related to the increased incidence of systemic abnormalities and retinal detachment，diagnosed by ultrasound, identified by CT, MRI ...
Shuang Zheng +7 more
semanticscholar +1 more source
European Journal of Ophthalmology, 2023
Purpose To describe a case of Bilateral Morning Glory Syndrome (MGS) associated with Unilateral Persistent Fetal Vasculature (PFV) in a 3-day old neonate.
H. Ran +7 more
semanticscholar +1 more source
Purpose To describe a case of Bilateral Morning Glory Syndrome (MGS) associated with Unilateral Persistent Fetal Vasculature (PFV) in a 3-day old neonate.
H. Ran +7 more
semanticscholar +1 more source
Morning Glory Syndrome With Bergmeister Papilla and Retinal Detachment.
JAMA ophthalmology, 2023This case report discusses a diagnosis of morning glory syndrome and concurrent Bergmeister papilla and retinal detachment in a child aged 3 years.
Guangwei Yu, Zhaoxia Zhai, Jinling Ge
semanticscholar +1 more source