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Risk of CNV related to angioid streaks in PXE

7 April 2021 | | EYE - Vitreo-Retinal
This retrospective cross-sectional study investigated 301 patients with pseudoxanthoma elasticum (PXE) for prevalence of choroidal neovascularisation (CNV) and macular atrophy. Some patients were excluded due to missing or poor-quality imaging or the fact that they didn’t have angioid streaks, leaving...

Clinical features and mortality of endogenous panophthalmitis in China

1 June 2022 | | EYE - Vitreo-Retinal | Endogenous endophthalmitis, Endogenous panophthalmitis, Interdisciplinary cooperation, Klebsiella pneumoniae, Pyogenic liver abscess
This longitudinal cohort study aimed to report the clinical features, treatment strategy, and mortality of 15 consecutive patients (16 eyes) with endogenous panophthalmitis (EP) at a tertiary medical centre of the largest eye centre in Northern China. Mean age was...
Strabismus journal front cover image.

Features, treatment and prevention of conjunctival inclusion cysts

10 May 2024 | | EYE - Paediatrics, EYE - Strabismus
Conjunctival inclusion cyst is a rare complication of strabismus surgery and generally develops at the point of muscle reattachment, caused by implantation of conjunctival epithelium. The authors aimed to determine the rate of its development after strabismus surgery and consider...
Eye journal cover image.

Nystagmus in infants (0–1 year)

2 October 2025 | | EYE - Vitreo-Retinal
This article from a tertiary hospital in Jerusalem documents the examination and investigations of 147 infants aged 0–1 years with nystagmus. The most common pathologies were albinism (59%) and inherited retinal dystrophy (IRD) (21%). They had eight patients with vertical...

The results of the last survey Oct21

1 October 2021 | | EYE - Cataract, EYE - Refractive, EYE - General
This edition’s survey questions moved away from the deep and ethically charged questions of the recent surveys and focussed on simple and straightforward issues. This is really where the surveys began in exploring the minor practice variations which we have...

What's trending Feb/Mar 2023

3 February 2023 | | EYE - General
A round-up of the eye related hot topics that have been trending on social media over the last few weeks. #nativity #needleeye Happy New Year! Let’s kick things off with a holiday-related story. Birmingham-based micro-engraver Graham Short engraved by hand...

Land Ahoy! An interview with Geoff Hilton-Barber

3 April 2026 | | EYE - General
It was during a previous interview with Miles Hilton-Barber [1] that I discovered that his older brother, Geoff, had been an inspiration to him. He informed me that Geoff was also blind from retinitis pigmentosa (RP) and had built his...

Gene Vision launched to support those diagnosed with genetic eye diseases

2 December 2020
A new website, Gene Vision (https://gene.vision), has been developed by Professor Mariya Moosajee and Dr Alex Yeong, supported by Dr Peter Thomas (Director of Digital Innovation at Moorfields Eye Hospital). The new site is intended for adults, children and their families who are diagnosed with rare genetic eye diseases.

College of Optometrists publishes guidance on GLP-1 weight loss drugs and vision

1 April 2026 | treatment, optometry, public health
GLP-1 weight loss drugs and vision: what clinicians need to know The College of Optometrists has issued guidance for clinicians following the publication of a recent MHRA drug safety update which has drawn attention to a very rare risk of...

An unusual presentation of sarcoidosis

1 October 2021 | | EYE - Vitreo-Retinal, EYE - Imaging, EYE - Neuro-ophthalmology, EYE - General
*Equally contributing co-first authors. Case report A 45-year-old man presented to his local optometrist with a three-week history of severe intermittent left eye pain with associated blurred vision and tenderness around his left temple. Two days prior, he developed weakness...

Genetic therapy gives infants life-changing improvements in sight

24 February 2025 | genetics, gene therapy, Moorfields, paediatrics, research, new, AIPL1, Leber Congenital Amaurosis
Four young children have gained life-changing improvements in sight following treatment with a pioneering new genetic medicine through Moorfields Eye Hospital and UCL Institute of Ophthalmology, with the support of MeiraGTx. The children were born with a severe impairment to...

The International AMD Genomics Consortium study: another success in understanding the complex genetics of AMD

1 April 2017 | | EYE - Vitreo-Retinal
Age-related macular degeneration (AMD) is a neurodegenerative complex disease of the eye and a major cause of blindness and visual impairment among the elderly worldwide. The early stages of the disease are characterised by asymptomatic pigmentary abnormalities and accumulation of...