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Renewed momentum in ocular gene and cell therapy, broadening application to chronic disease

Gene and cell therapies offer the prospect of ground-breaking new avenues for the treatment of diseases, reflected in a renewed explosion of interest and investment in retinal gene therapy. Rod McNeil reports recent clinical trial readouts across a diverse range...

Cavernous sinus syndrome

Anatomically the cavernous sinus is a plexus of multiple veins that are connected and within this plexus there are several important vascular and neurological structures. These include cranial nerves III, IV, V1 (and sometimes V2), VI as well as the...

Q&A: Mr Goel and Mr Loomba on alcohol delamination and phototherapeutic keratectomy (PTK) for the treatment of recurrent corneal erosion syndrome

Recurrent corneal erosion syndrome is a common, recurrent condition caused by abnormal epithelial adhesion to the underlying basal lamina. Spontaneous breakdown of the corneal epithelium can lead to the sudden onset of ocular pain, blurred vision, tearing and photophobia, typically...

Exotropic Moebius syndrome

Three patients are described with pattern C Moebius syndrome and report the technique and outcomes of surgery for two patients. The three cases included a three and a 13-year-old requiring surgery and a 10-year-old. All patients had absent horizontal gaze...

A case report of bidirectional aberrant upward eye movement

The authors present a case report of a 14-year-old boy with left ptosis and strabismus since childhood. In primary position he had left hypotropia with ptosis. On elevation of the right eye, the left eye depresses and adducts. Conversely, on...

Ocular neuromyotonia

The authors report a cohort of ten patients (nine female) with ocular neuromyotonia (ONM) for clinical signs and symptoms, treatment methods and outcome. Six had affected vertical muscles including superior oblique, inferior rectus and superior rectus. Four had affected lateral...

Genetic profiles of primary strabismus

The authors explore the pedigree analysis of familial cases of primary concomitant strabismus (PCS) to unravel the genetic determinants of this strabismus. Of 2301 cases of PCS, 39 (1.7%) had familial clustering. This study recruited 18 families with esotropia and...

Veterans with vision impairment deserve better public transport links says Paisley Councillor

Cllr Carolann Davidson, Labour & Cooperative Councillor for Paisley East and Central, recently visited Sight Scotland Veterans’ Hawkhead Centre to see first-hand the great work the charity does in supporting veterans with sight loss.

Worshipful Company of Spectacle Makers awards silver Fincham medal to Professor Shahina Pardhan

The Worshipful Company of Spectacle Makers has demonstrated its continuing support for research by awarding its prestigious Silver Medal to Professor Shahina Pardhan, the UK’s first female Professor of Optometry, and by renewing its commitment to further medal awards for academic and clinical achievement.

Nikolaos Koutris takes on half marathon to raise awareness for Sight Scotland and high eye pressure

Nikolaos Koutris, 37, originally from Greece and now residing in Edinburgh, has been inspired to run a half marathon for Sight Scotland after being diagnosed with high eye pressure.

Mapping the Future of Vision Impairment Services in Scotland

Vision Collaborative Scotland, formerly the Scottish Vision Services Steering Group, has re-launched with a new name, a renewed purpose, and an ambitious vision. Now known as Vision Collaborative Scotland, the group of third sector partners is committed to transforming the...

Researchers identify a novel genetic cause of Fuchs endothelial corneal dystrophy

Researchers identify a novel genetic cause of Fuchs endothelial corneal dystrophy, offering new ways for future therapies to target this common, age-related cause of visual loss. In a landmark study, researchers supported by NIHR Moorfields Biomedical Research Centre, have identified...