A case of morning glory syndrome associated with persistent hyperplastic primary vitreous and Peters’ anomaly [PDF]
GMS Ophthalmology Cases, 2017 We report a case of morning glory syndrome (MGS) associated with persistent hyperplastic primary vitreous (PHPV) and Peters’ anomaly. A 2-day-old girl, born at term with a birth weight of 3,350 g was diagnosed with Peters’ anomaly, cataract ...
Muslubas, Isil Sayman +3 more
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Basal encephalocele associated with morning glory syndrome: case report Encefalocele basal associada a síndrome "morning glory": relato de caso [PDF]
Arquivos de Neuro-Psiquiatria, 2007 The basal encephaloceles refer to rare entities and they correspond to herniation of brain tissue through defects of skull along the cribiform plate or the sphenoid bone. A rare morning glory syndrome, with characteristic retinal defect has been reported
Ivanete Minotto +5 more
doaj +2 more sources
Clinical characteristics and strabismus patterns in 61 patients with morning glory syndrome: a retrospective study [PDF]
BMC OphthalmologyBackground To analyze the frequency, type distribution, and related clinical characteristics of strabismus in patients with morning glory syndrome, and to provide evidence for clinical evaluation and intervention.
Congqi Li +5 more
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Bilateral Morning Glory Syndrome with Bilateral Persistent Fetal Vasculature in a Patient with Joubert’s Syndrome [PDF]
Case Reports in Medicine, 2020 Purpose. We report a case of a 1-year-old girl who was referred to us with a cerebellar anomaly and delayed growth and development for bilateral ptosis and poor fixation.
Ahmad Bilal Araissi +2 more
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Morning Glory Syndrome associated with Autosomal Dominant Alport Syndrome with a Heterozygous Mutation [PDF]
Childhood 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 +3 more sources
Morning glory syndrome with Moyamoya disease: A rare association with role of imaging [PDF]
Indian Journal of Radiology and Imaging, 2018 Morning glory disc anomaly (MGDA) is a congenital optic nerve anomaly characterized by a funnel-shaped excavation of the posterior globe that incorporates the optic disc. Most cases are isolated and not associated with systemic anomalies.
Janardhana Ponnatapura
doaj +2 more sources
Intraoperative optical coherence tomography assisted analysis of pars Plana vitrectomy for retinal detachment in morning glory syndrome: a case report [PDF]
BMC Ophthalmology, 2017 Background The pathogenesis of non-rhegmatogenous retinal detachment (non-RRD) associated with morning glory syndrome (MGS) is not established, as well as best surgical approach to treat RD.
Lyubomyr M. Lytvynchuk +3 more
doaj +2 more sources
Patient with Morning Glory syndrome [PDF]
Einstein (São Paulo), 2015 Thiago Gonçalves dos Santos Martins +2 more
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Contractile morning glory disc anomaly associated with total retinal detachment: a case report [PDF]
BMC OphthalmologyBackground Morning glory disc anomaly is a rare congenital optic nerve head malformation. The contractile variant, characterized by rhythmic pulsatile movement of the optic disc, is exceptionally uncommon, and detailed documentation of its dynamic ...
Chengzhi Liu +4 more
doaj +2 more sources
Persisting Embryonal Infundibular Recess in Morning Glory Syndrome: Clinical Report of a Novel Association. [PDF]
AJNR Am J Neuroradiol, 2019 Morning glory syndrome is characterized by a congenital optic disc defect that resembles the eponymous flower. We present the MR imaging findings of 2 pediatric patients with morning glory disc anomaly and persisting embryonal infundibular recess ...
D'Amico A +6 more
europepmc +2 more sources