Results 41 to 50 of about 14,669 (176)

Basal encephalocele associated with morning glory syndrome: case report Encefalocele basal associada a síndrome "morning glory": relato de caso

open access: yesArquivos 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   +1 more source

Isolated Sporadic Morning Glory Syndrome A Rare Entity

open access: yesDelhi Journal of Ophthalmology, 2012
Morning Glory syndrome is diagnosed by whitish glial tissue at the bottom of the disk with retinal blood vessels emerging from the periphery of the excavation in a radial pattern.
Priya Dua, Amar Dev, Akash Dua
doaj   +1 more source

Morning Glory Disc Anomaly, A Report of a Successfully Treated Case of Functional Amblyopia [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Morning Glory Disc Anomaly (MGDA) is a congenital malformation of the optic nerve characterized by the presence of a funnel-shaped macropapilla with neuroglial remnants in its center surrounded by an elevated and pigmented chorioretinal ring.
Humberto Cavazos-Adame   +3 more
doaj   +1 more source

Rarely seen optic disc anomaly: a case of Morning Glory Syndrome

open access: yesAnkyra Medical Journal
Morning Glory Syndrome (MGS) is a rare optic nerve anomaly, typically unilateral, characterized by a funnel-shaped macropapilla with neuroglial remnants at its center, surrounded by an elevated and pigmented chorioretinal ring.
Mustafa Bülbül   +2 more
semanticscholar   +1 more source

A Case of Moyamoya Disease in Morning Glory Syndrome

open access: yesJournal of the Korean Ophthalmological Society
Purpose: We report a diagnosis of Moyamoya disease based on brain magnetic resonance imaging (MRI) and brain magnetic resonance angiography (MRA) performed in a child diagnosed with morning glory syndrome.Case summary: A 6-year-old boy visited the ...
J. Byun, Se Youp Lee, S. Cho
semanticscholar   +1 more source

Seizures in children with Dravet syndrome in extreme heat: A qualitative study of parental perspectives

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Perspectives of parents of children with Dravet syndrome indicate that extreme heat and high temperatures exacerbate epileptic seizures, introduce new seizure triggers, and require the adoption of specific seizure‑management strategies. Abstract Aim To describe parental perspectives on how heatwaves and high ambient temperatures influence seizure ...
Angel Aledo‐Serrano   +8 more
wiley   +1 more source

Case Report: Fibroglial Retinal Tissue in Contractile Morning Glory Disc Anomaly

open access: yesCase Reports in Ophthalmology, 2021
The purpose of the present case is to describe a patient with tractional retinal detachment (RD) associated with contractile morning glory: a 17-year-old female, with a history of failed surgery for RD when she was 2 years old in her right eye (OD ...
Abel Ramirez-Estudillo   +5 more
doaj   +1 more source

Clinical outcomes of mitochondrial‐enhancing nutraceutical supplementation in psychiatric disorders: A systematic review

open access: yesGeneral Psychiatry, Volume 39, Issue 3, June 2026.
ABSTRACT Background Nutraceutical supplementation targeting mitochondrial function has been proposed as a beneficial therapeutic strategy to improve physical and mental health in psychiatric patients. Aims To summarise the results of studies evaluating nutraceutical supplementation targeting mitochondrial function in patients with psychiatric disorders.
Juan Tortajada   +9 more
wiley   +1 more source

MORNING GLORY SYNDROME:A RARE ENTITY

open access: yesInternational Journal of Advanced Research
Morning glory syndrome is a rare congenital optic disc anomaly that can cause visual impairment and may be linked to ocular and non-ocular abnormalities. It is characterized by a distinct fundoscopic appearance, which includes a large excavated disc with
Jitendra Kumar, Shikha Tolia, Amit Rao
semanticscholar   +1 more source

Vitreoretinal complications and surgical outcomes in patients with X‐linked retinoschisis

open access: yesActa Ophthalmologica, Volume 104, Issue 4, Page 410-422, June 2026.
Abstract Purpose X‐linked retinoschisis (XLRS) is an inherited vitreoretinal disorder characterized by macular retinoschisis. In a subgroup of patients, peripheral retinoschisis can occur, potentially leading to complications such as vitreous haemorrhage (VH) and retinal detachment (RD).
Jonathan Hensman   +11 more
wiley   +1 more source

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