Results 41 to 50 of about 835,973 (179)

Capillary haemangiomas in association with morning glory disc anomaly [PDF]

open access: yesActa Ophthalmologica Scandinavica, 1998
Capillary haemangiomas in children are usually isolated, but may have systemic associations. This accords with our finding of ocular malformations, especially "morning glory disc anomaly" (MGDA), in three children which are described.All three children had extensive capillary haemangiomas in combination with MGDA in one eye.
G, Holmström, D, Taylor
openaire   +2 more sources

Morning Glory Syndrome associated with Autosomal Dominant Alport Syndrome with a Heterozygous Mutation [PDF]

open access: yesChildhood Kidney Diseases, 2021
Morning glory syndrome (MGS) is a rare congenital optic disc anomaly with a characteristic fundal finding with severe visual impairment. It may occur in association with various systemic manifestations, even though most of the reported cases were ...
So Jeong Kim   +7 more
doaj   +1 more source

Синдром на “MORNING GLORY”- Приказ на случај

open access: yes, 2022
Morning Glory Syndrome (MGS) is an uncommon congenital anomaly of the eye nerve (optic nerve) that resembles a flower known as morning glory, impairs vision, and may be associated with both ocular and non-ocular abnormalities.
Isjanovski, Igor   +3 more
core   +1 more source

An unusual association of Morning Glory Syndrome with chronic myeloid leukemia-Philadelphia chromosome

open access: yesJournal of Family Medicine and Primary Care, 2020
Morning glory disc anomaly (MGDA) is a rare congenital malformation that results from the incomplete formation of the optic nerve in utero. The majority of the patients have unilateral involvement and poor vision leading to sensory strabismus.
Rakesh Panyala   +3 more
doaj   +1 more source

Macular Hole in Morning Glory Syndrome: A Case Report and Review of Literature [PDF]

open access: yes, 2022
Morning glory syndrome is a rare congenital excavated optic disc anomaly that can impair vision and may be associated with ocular and non-ocular abnormalities.
Zare Mehrjardi, Alireza   +2 more
core   +1 more source

Postoperative follow-up of a case of atypical morning glory syndrome associated with persistent fetal vasculature

open access: yesBMC Ophthalmology, 2019
Background Morning glory syndrome is a relatively rare congenital optic disc anomaly that is often difficult to identify when associated with additional congenital ocular anomalies.
Heng Jiang   +3 more
doaj   +1 more source

Morning Glory Disc Anomaly

open access: yes, 2023
A colored fundus photo of a patient with morning glory anomaly. Morning glory anomaly is a rare congenital malformation of the optic nerve. The morning glory disc anomaly can be seen with transsphenoidal basal encephalocele.
Bashaer Aldhahwani, MD; Carlos Ernesto Mendoza Santiesteban, MD
core  

Morning Glory Anomaly in A Fifteen-Year-Old Saudi Girl [PDF]

open access: yesInternational Journal of Medical Arts
Background: The Morning Glory anomaly is an extremely unusual birth defect affecting the optic disc.  It may exist in isolation or in conjunction with other ocular or non-ocular malformations.
Ahmed El Sayegh   +2 more
doaj   +1 more source

Total retinal detachment and contractile movement of the disc in eyes with morning glory syndrome

open access: yesAmerican Journal of Ophthalmology Case Reports, 2020
Purpose: This study aimed to report clinical characteristics, intraoperative findings, and surgical outcomes of 2 eyes of 2 patients with retinal detachment (RD) associated with morning glory syndrome (MGS) and contractile movement of the disc ...
Masuo Sakamoto   +4 more
doaj   +1 more source

Morning glory syndrome associated with primary open angle glaucoma: Case report [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2014
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 ...
Božić Marija   +3 more
doaj   +1 more source

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