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Cytomegalovirus retinitis post intravitreal triamcinolone in an immunocompetent patient with juvenile glaucoma

Figure 1: Fundus photograph shows active CMV retinitis four weeks after IVTA in the right eye. Figure 2: Fundus photograph of the left eye with no CMV retinitis; atrophic disc as a result of juvenile glaucoma. Case report A 29-year-old...

Cortical blindness

Cortical blindness is a rare but recognised entity. Cerebrovascular accident is a well-known risk factor. We report a case of an 84-year-old lady with bilateral cortical blindness with multiple cardiovascular risk factors. Case report An 84-year-old lady was admitted under...

Refractive surprise after cataract surgery caused by posterior capsular striae

Cataract removal with intraocular lens (IOL) implantation is one of the most frequently performed surgeries in current clinical practice [1,2]. New microsurgical techniques and refined IOL power calculations allow excellent refractive outcomes. Refractive surprise following cataract surgery is uncommon [1-3]...

Glaucoma UK Fellow receives international research award

Dr Giovanni Montesano, the Glaucoma UK Pitts Crick Fellow, has been awarded an ARVO Foundation Early Career Clinician-Scientist Research Award in recognition of his outstanding work in vision research. The award celebrates early career clinician-scientists whose research is shaping the...

Artificial intelligence could transform patient education in eyecare

A multilingual, voice-enabled chatbot helps patients access retinal detachment advice through personalised, real-time, clinically grounded conversations. From hospital leaflets to spoken answers in dozens of languages, new research from the University of East London (UEL) suggests artificial intelligence could dramatically...

Countdown to opening begins as NHS takes keys for new Sunderland Specialist Eye Hospital

Leaders at South Tyneside and Sunderland NHS Foundation Trust today took their first steps inside the region’s new specialist eye hospital as construction partner Kier officially handed over the keys. Set to open later this summer, NHS leaders have also...

Redefining the future of sight - Moorfields Eye Charity launches first major national funding initiative

New grants strategy aims to enable innovation at scale and transform eye health. Moorfields Eye Charity has launched a significant national funding initiative to accelerate the urgent development of new eye health treatments and interventions. The new Discovery and Translation...

Ocular toxicity secondary to deferoxamine

Patients with myelodysplastic syndromes can develop transfusion-related iron overload as they become dependent on recurrent blood transfusions [1]. Iron chelation therapy is indicated for the treatment of iron overload and one established example of this is deferoxamine. However, deferoxamine ocular...

Fusarium keratitis in a patient with alcohol dependence

Treatment of fungal keratitis secondary to the Fusarium species remains a challenge. Although relatively more common in warmer climates, this corneal infection is rare in the UK. Most cases have been reported in farmers and are often preceded by trauma....

Glaucoma UK announces winners of the 2025 ‘Excellence in Glaucoma Care Award’

Glaucoma UK is delighted to announce the winners of this year's Excellence in Glaucoma Care Awards – Patrick (Paddy) Gunn from Manchester and Alex Gage Family Optometrists in Sheffield. This annual award celebrates individuals or teams who have made remarkable...

UK Eye Care Data Hub updated with additional eye conditions

The UK Eye Care Data Hub, the most up-to-date and comprehensive model of the UK’s eyecare workforce and eye diseases in one place, has been expanded to almost double the number of eye conditions and update aspects of the sector...

Treatment for cause of sudden sight loss now available through the NHS in England

The National Institute for Health and Care Excellence (NICE) has approved a treatment for Leber Hereditary Optic Neuropathy (LHON), called Idebenone (Raxone), in those aged 12 and above who are affected by the condition. LHON is a rare mitochondrial genetic...