You searched for "vision"
Clear sight is ‘revelation’ for Yaxley resident following ‘life-changing’ surgery
Retiree Steve Low has rekindled his love for photography.Embracing assistive technology in the fight against sight loss
The author shares his own experience of sight loss and explains the vital role assistive technology can play in the lives of visually impaired patients. There is no doubt that sight loss continues to be a clear and present danger,...Light in darkness – manual small incision cataract surgery in India
Cataract has been documented to be the most significant cause of bilateral blindness in India, where vision <20/200 in the better eye on presentation is defined as blindness [1,2]. Estimation of blindness in India by the World Health Organization (WHO)...Blind veterans continue hillwalking passion thanks to power of VR
Imagine being a keen hillwalker who loves the outdoors but then being unable to enjoy it because of sight loss. Fortunately, many veterans of the Armed Forces who have visual impairment can climb their favourite mountains again, thanks to Sight Scotland Veterans.250 QFFD bicycles make sight saving care possible in rural Zambia
Sight-saving charity Orbis, is delivering a project in the Copperbelt province of Zambia, tackling the difficulties of delivering eye care in rural areas by providing 250 bikes to Community Eye Health Champions (CEHCs).Apr/May 2015 Quiz
History A 60-year-old man presented to the ophthalmologists with painful blurred left vision. Examination revealed a white vascular mass, occupying 60% of the anterior chamber space, arising from the iris. After conservative therapy, no useful vision remained. The eye was...
Intravitreal afibercept and ranibizumab for PCV
This is a retrospective, interventional series comprising 98 eyes with polypidal choroidal vasculopathy (PCV) with the aim of comparing treatments with afibercept and ranibizumab, highlighting any differences in their efficacy. Case notes and imaging (FFA / ICG / OCT) were...Neurofibromatosis type 2 – diagnosis, features and MDT approach
NF2 is a genetic condition caused by mutation in a single gene (NF2 gene) on chromosome 22. The NF2 gene provides instructions to produce a protein called merlin, also known as schwannomin. This protein functions as a tumour suppressor, preventing...
Corneal crosslinking in pellucid marginal degeneration
Fourteen studies were included in this first review examining the use of corneal-crosslinking (CXL) to treat pellucid marginal degeneration (PMD). PMD is a bilateral, non-inflammatory corneal thinning disorder characterised by inferior peripheral corneal thinning 1-3mm from the limbus in the...
CHARGE syndrome features
CHARGE syndrome (CS) includes coloboma, heart defects, atresia of the choanae, retardation of growth and development, genital and urinary anomalies and ear anomalies. The authors developed an original self-administered questionnaire (VISIOcharge) for patients with CS and used it to evaluate...
