ÁñÁ«ÊÓƵ

This systematic review and meta-analysis evaluates associations of common single-nucleotide variants and rare coding variants with primary angle-closure disease.

This study describes the adoption of bias reduction practices in underrepresented groups in ophthalmology residency recruitment and attempts to determines which practices are effective for increasing these residents.

A 37-year-old woman was referred for evaluation of a retinal detachment in her left eye. Posterior examination results demonstrated a retinal detachment in the posterior pole with shifting fluid and no identifiable retinal break, and there was a thickened choroid with a hyporeflective band on ultrasound biomicroscopy. What would you do next?

This case report describes a patient with attenuation of retinal arterioles and veins associated with 2 blot hemorrhages and pallor of the inferotemporal retina without emboli.

This case series describes the clinical course, outcomes, and microbiological diagnostic profiles of multidrug-resistant Pseudomonas aeruginosa keratitis and the use of rose bengal–photodynamic antimicrobial therapy as an alternative or adjunctive therapy to treat isolates.

This extension of the Trial of Overminus Spectacle Therapy for Intermittent Exotropia compares refractive error change over 3 years in children with intermittent exotropia originally treated with overminus vs nonoverminus spectacles.

This Special Communication discusses a research-informed consent framework for posthumous whole-eye donation.

This article discusses treatment options for suspects of primary angle-closure disease.

A 38-year-old man had an asymptomatic, orange, macular choroidal mass with macular choroidal folds and a retinal pigment epithelial detachment in the right eye and a second orange mass nasal to the optic disc also in the right eye. What would you do next?