Results 31 to 40 of about 14,669 (176)
A case of morning glory syndrome
PAMJ Clinical Medicine, 2022 Islam Bechakh, Abdelhakim Hammoudi
openaire +2 more sources
Human Amniotic Membrane: A Seal for Complex Retinal Detachments [PDF]
Türk Oftalmoloji DergisiObjectives: To evaluate the efficacy of human amniotic membrane (hAM) transplantation for complex retinal detachments (RD). Materials and Methods: A retrospective analysis of consecutive patients who underwent vitreoretinal surgery with hAM ...
Ece Özdemir Zeydanlı +3 more
doaj +2 more sources
Morning glory syndrome associated with primary open angle glaucoma: Case report [PDF]
Srpski 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
JBNC - JORNAL BRASILEIRO DE NEUROCIRURGIA, 2018 Morning Glory Syndrome is a very rare condition. It is characterized by an enlarged and funnel-shaped optic disc excavated and is associated with other craniofacial anomalies such as hypertelorism, cleft lip, cleft palate, and basal encephalocele. CaseReport.
Moysés Isaac Cohen +10 more
+5 more sources
Management of Retinal Detachment Associated with Morning Glory Disc Syndrome
Case Reports in Ophthalmology, 2021 We report a case of morning glory disc anomaly in a young patient with tractional retinal detachment successfully repaired with complex pars plana vitrectomy, membrane peel, laser, and oil tamponade.
Tyler Etheridge +2 more
doaj +1 more source
A Rare Case Report of Morning Glory Syndrome in North Karnataka, Vijayapura
BLDE University Journal of Health Sciences, 2020 Background: Morning Glory Syndrome is a rare congenital optic disc anomaly. The etiology of the disorder remains controversial and unclear. It is uncommon and can be either isolated or associated with malformations.
Sunil Biradar, Magna Mary Kuruvila
doaj +1 more source
A Case of Renal Coloboma Syndrome Caused by Spontaneous Mutation of PAX2
罕见病研究, 2022 This article reports a case of a child with full-length (paired box family, PAX) PAX2 mutation leading to renal coloboma syndrome. The patient is an 11-year-old boy presented with persistent foamy urine and unexplained renal failure.
LING Chen, CHEN Zhi, LIU Xiaorong
doaj +1 more source
Retinal cases & brief reports, 2022 Supplemental Digital Content is Available in the Text. A case of morning glory syndrome complicated by a macula-off retinal detachment treated with a human amniotic membrane patch positioned onto the optic nerve defect and silicone oil endotamponade is ...
T. Caporossi +6 more
semanticscholar +1 more source