Case report from SECO 2026 shows how a rare blood disorder can be an atypical cause of nonarteritic anterior ischemic optic neuropathy.

Congenital aniridia is a rare disease caused, in most cases, by mutations in the PAX6 gene, which is essential for the development of ocular structures.

A secondary stress signaling pathway in the response to optic axon injury is an unexpectedly strong contributor to both neurodegeneration and axon regenerative potential.

Millions of people around the world take medicine every day to control high blood pressure. These medicines help protect the heart, brain, and blood vessels from serious problems such as heart attacks ...

Lifestyle diseases and screen habits are silently impacting eye health in urban India. Learn why awareness and timely eye ...

Blurry vision isn’t always due to screen strain or ageing. Ophthalmologists warn it can signal vitamin deficiencies like A, B12, D, or E, affecting the retina and optic nerve. Symptoms include night ...

LOVELAND, CO - January 27, 2026 - PRESSADVANTAGE - As awareness grows around early detection and management of ...

Billings, MT - January 26, 2026 - PRESSADVANTAGE - Patients seeking expert care for glaucoma in the region are turning ...

Glaucoma is often called the “silent thief of sight”, and for good reason. Millions live with this condition without even ...

According to recent data, patients initiating semaglutide had a substantially greater risk of developing NAION versus those starting SGLT2 inhibitors. Although rare, semaglutide initiation can lead to ...

Veterans with type 2 diabetes who are initiating semaglutide appear to have double the NAION risk compared with those starting SGLT2 inhibitors.

CEDAR RAPIDS, IA - January 27, 2026 - PRESSADVANTAGE - As cases of glaucoma continue to rise across the United States, ...