Results 31 to 40 of about 13,874 (208)

Acute macular neuroretinopathy associated with intravitreal anti-VEGF injection: A case report

American Journal of Ophthalmology Case Reports, 2022
Purpose: to report a case of acute macular neuroretinopathy occurring after intravitreal aflibercept injection for macular edema due to CRVO. Observations: Two days after Aflibercept intravitreal injection, the patient developed vision loss associated ...
Loubna M. Radwan, Ghazi O. Bou Ghanem, Ghassan N. Daye, Nicola G. Ghazi   +3 more
doaj   +1 more source

Electrophysiological abnormalities associated with extensive myelinated retinal nerve fibers

Indian Journal of Ophthalmology, 2012
An observational case report of electrophysiological abnormalities in a patient with anisomyopic amblyopia as a result of unilateral extensive myelinated retinal nerve fibers (MNFs) is illustrated.
Su Ann Tay, Srinivasan Sanjay
doaj   +1 more source

Isolated homonymous hemianopsia due to presumptive cerebral tubercular abscess as the initial manifestation of human immunodeficiency virus infection

Indian Journal of Ophthalmology, 2012
We report a case of isolated homonymous hemianopsia due to presumptive cerebral tubercular abscess as the initial manifestation of human immunodeficiency virus (HIV) infection.
Sujit Gharai, Pradeep Venkatesh, Anindita Sinha, Satpal Garg, Prapti Ghosh   +4 more
doaj   +1 more source

Filling-in of the foveal blue scotoma [PDF]

, 2001
The blue-blindness (tritanopia) of the human foveola normally goes unnoticed but can be directly visualized by having observers view a flickering, monochromatic, short-wavelength field.
Spillmann, Lothar, Werner, John S, Magnussen, Svein, Stürzel, Frank, Werner, John S.   +4 more
core   +1 more source

Functional evaluation of the macular area in early glaucoma using microperimetry

Indian Journal of Ophthalmology, 2021
Purpose: To evaluate the central visual field by microperimetry (MP), in early glaucoma. Methods: Consecutive perimetrically experienced patients with a single nasal step or arcuate scotoma and 14 control eyes underwent MP.
Swati Phuljhele, Dewang Angmo, Lalit Aalok, Sandeep Parwal, Raj Vardhan Azad, Viney Gupta, Ramanjit Sihota   +6 more
doaj   +1 more source

Simulated scotoma with assistive technology for diabetic retinopathy

Array
This research presents a literature review and a novel contribution in assistive technology for scotoma blind spots. This review covers recent developments in: (i) simulation of blind spots, (ii) search tasks with blind spots, (iii) reading with ...
Neil Vaughan
doaj   +1 more source

Homonymous hemianopsia: Case report [PDF]

ABC: časopis urgentne medicine, 2018
Introduction: Cerebrovascular diseases include a wide range of diseases and disorders based on damage to the blood vessels of the brain. Disorders in the visual field can be caused by various neurological and ocular diseases.
Repac Vinka J., Vlatković Zoranka M., Repac Marija M.   +2 more
doaj  

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto, Céline Huber, Clément Paya, Isabelle Audo, Nathalie Boddaert, Valérie Cormier‐Daire   +5 more
wiley   +1 more source

Investigated layers related to scotoma location.

, 2018
Box-and-whisker plots of the mean thickness of RNFL, GCL and IPL in glaucoma eyes investigated with reference to the localization of the absolute visual field scotoma.
Matus Rehak (6166922), Michael R. R. Böhm (5316044), Franziska G. Rauscher (275505), Jan D. Unterlauft (6166919)   +3 more
core   +1 more source

Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes

Epilepsia Open, EarlyView.
Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola, Marica Rubino, Antonella Riva, Pasquale Striano   +3 more
wiley   +1 more source