Results 21 to 30 of about 2,592 (175)

Morning glory disc anomaly with contractile movements. [PDF]

open access: yesGraefes Arch Clin Exp Ophthalmol, 2012
Morning glory disc anomaly is a rare malformation characterized by an ectasia of the posterior pole of the fundus involving the optic disc. Embryologically, there are some theories for its pathogenesis, including primary mesenchymal abnormality, defective closure of the embryonic fissure, and basic defect of mesoderm combined with dynamic disturbance ...
Sawada Y, Fujiwara T, Yoshitomi T.
europepmc   +4 more sources

MRI Evaluation of Vasculopathy and Additional Intracranial Manifestations in Morning Glory Disc Anomaly [PDF]

open access: yesThe Journal of Pediatric Academy
Morning glory disc anomaly (MGDA) is rare, but its fundoscopic findings are well documented in the ophthalmologic literature. It is sporadic, without sexual predisposition, and usually unilateral.
Gordon David Heller   +1 more
doaj   +3 more sources

Internal carotid artery origin of the anterior cerebral artery: A rare anatomic intracranial arterial variation in a child with morning glory disc anomaly and moyamoya vascular pattern; case report and review of literature [PDF]

open access: yesBrain Circulation, 2020
Morning glory disc anomaly (MGDA) characterizes a congenital dysgenetic disorder of the optic disc, coexisting with arterial intracranial abnormalities, including Moyamoya vascular disease, a significantly rare disease in the European populations.
Aikaterini Solomou   +4 more
doaj   +2 more sources

Morning glory disc anomaly and facial hemangiomas in a girl with moyamoya syndrome

open access: yesIndian Journal of Ophthalmology, 2018
Moyamoya disease (MMD) is a chronic progressive, occlusive cerebrovascular disease in the circle of Willis and the feeding arteries. Morning glory disc anomaly (MGDA) is characterized by an abnormal excavated optic disc with radial emergence of blood ...
Sanitha Sathyan, Mariea Chackochan
doaj   +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   +3 more sources

A Rare Case of Unilateral Morning Glory Disc Anomaly in a Patient with Turner Syndrome: Report and Review of Posterior Segment Associations [PDF]

open access: yesCase Reports in Ophthalmological Medicine, 2018
Turner syndrome is a common sex chromosome disorder affecting females. The disorder is caused by a partial loss, complete absence, or structural abnormality of one X chromosome.
Dev R. Sahni   +4 more
doaj   +2 more sources

Bilateral morning glory disc anomaly.

open access: yesIndian Journal of Ophthalmology, 2003
Morning glory disc anomaly (MGDA) is usually known to be unilateral. We report an unusual case of a bilateral form of the disorder with an aim to distinguish it from other bilateral optic nerve head anomalies.
Deb Nilanjana, Das Rita, Roy I
doaj   +2 more sources

Refractive Error Correction With Glasses in Congenital Ocular Fundus Anomalies: A Retrospective Series of 18 Children With Different Disease Entities Followed Up for More Than 10 Years. [PDF]

open access: yesCureus
Objectives: Children with congenital anomalies of the posterior segment of the eye are in the process of visual development, and thus, their refractive errors should be detected by cycloplegic refraction testing to prescribe full-correction glasses, if ...
Matsuo T.
europepmc   +3 more sources

Congenital malformations of the eye: a pictorial review and clinico-radiological correlations [PDF]

open access: yesJournal of Ophthalmology, Volume 2024, Issue 1, 2024.
Congenital malformations of the eye represent a wide and heterogeneous spectrum of abnormalities that may be part of a complex syndrome or be isolated.
Carboni A.   +12 more
core   +2 more sources

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