Results 1 to 10 of about 25,913 (280)

Corneal and scleral biomechanics in ophthalmic diseases: An updated review

open access: goldMedicine in Novel Technology and Devices, 2022
Corneal and scleral biomechanical properties have important implications in the maintenance of normal ocular morphology and function. The cornea and sclera compose the outermost layer of the eyeball, forming a sphere with a certain degree of intraocular ...
Yan Wang, Huazheng Cao
doaj   +3 more sources

Large diameter scleral lens benefits for Asians with intractable ocular surface diseases: a prospective, single-arm clinical trial [PDF]

open access: goldScientific Reports, 2021
To report the efficacy and safety of large diameter scleral lenses and determine their suitability in Asian subjects with intractable ocular surface diseases.
Jayoon Moon   +5 more
doaj   +2 more sources

Clinical Use of Mini-Scleral Contact Lens in Ocular Surface Diseases [PDF]

open access: hybridAnnals of Optometry and Contact Lens, 2022
A scleral contact lens lies on the sclera, not the cornea, which differs from a rigid gas permeable (RGP) contact lens, and has shown successful clinical outcomes in patients unable to tolerate glasses or RGP contact lenses because of a severely deformed cornea.
Seung Ahn Yang, Su Hwan Park, Ji Eun Lee
openaire   +2 more sources

Whipple’s disease scleral nodules: a novel presentation in 2 consecutive patients [PDF]

open access: goldBMC Ophthalmology, 2020
Abstract Background Whipple’s disease (WD) is a rare, chronic, infection caused by gram-positive filamentous aerobic actinobacterium Tropheryma whipplei occurs classically in the gastrointestinal tract and shows histopathologically foamy macrophages with typical numerous PAS-positive, non-acid fast particles.
Waleed K. Alsarhani   +5 more
openaire   +4 more sources

IgG4-related disease presenting as panuveitis without scleral involvement [PDF]

open access: goldJournal of Ophthalmic Inflammation and Infection, 2017
The following case emphasizes the importance of including IgG4-related disease (RD) in the differential diagnosis of intraocular inflammation and multiple cranial nerve palsies.A 33-year-old man, with a history of idiopathic bilateral panuveitis, presented with a new right pupillary-sparing partial third nerve palsy, which spontaneously resolved in 2 ...
Kinda Najem   +2 more
openaire   +4 more sources

Prescription Habits of Scleral Lenses for the Management of Corneal Irregularity and Ocular Surface Disease Among Scleral Lens Practitioners

open access: greenEye & Contact Lens: Science & Clinical Practice, 2022
Objectives: To describe prescribing patterns of therapeutic scleral lenses (SLs) in the management of corneal irregularity and ocular surface disease among practitioners who prescribe SLs. Methods: Participants ranked treatment options for corneal irregularity and ocular surface ...
Ellen Shorter   +5 more
openaire   +4 more sources

Indications of Scleral Contact Lenses in Ocular Surface Diseases

open access: goldJournal of Optometry and Ophthalmology, 2021
The use of scleral lenses is increased over the last decade. Not only it helps in the patient’s visual rehabilitation but also provides wearing comfort to the patient. Previously scleral lenses were mostly prescribed in cases where traditional therapies don’t work well.
Sudhanshu Dhanotia
openaire   +2 more sources

Endothelial dysfunction after scleral lens use in patients with herpetic eye disease [PDF]

open access: bronzeCanadian Journal of Ophthalmology, 2020
Abstract Objective To assess the impact of scleral contact lens use on corneal endothelial cell function in eyes previously infected with the herpes viridae family of viruses. Design Retrospective review of four patient charts. Participants Four patient charts for a total of 6 eyes were included in this study. 50% of participants were female,
Jaime C. Sklar   +3 more
openaire   +3 more sources

Deep Scleral Exposure: A Degenerative Outcome of End-Stage Stargardt Disease [PDF]

open access: greenAmerican Journal of Ophthalmology, 2018
To describe a distinct phenotypic outcome of outer retinal degeneration in a cohort of genetically confirmed patients with recessive Stargardt disease (STGD1).Retrospective case series.Twelve patients, who were clinically diagnosed with STGD1 and exhibited a unique degenerative phenotype, were included in the study.
Winston, Lee   +4 more
openaire   +4 more sources

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