In the realm of ophthalmology, CRISPR-Cas technology emerges as a transformative force, promising bespoke treatments for a spectrum of ocular ailments. With its precision gene-editing capabilities, CRISPR holds the potential to correct the genetic anomalies underlying inherited retinal diseases like retinitis pigmentosa and Leber congenital amaurosis. Beyond mere correction, it opens avenues for personalized medicine, paving the way for tailored therapies based on an individual's genetic makeup. Despite its immense promise, hurdles such as off-target effects and delivery mechanisms necessitate careful navigation. Nonetheless, CRISPR stands poised to reshape the landscape of ocular care, offering a glimmer of hope to those grappling with vision loss due to currently untreatable conditions.







Title : Why a paediatric orthoptic oncology service matters
Shenika Tailor, University Hospitals of Leicester NHS Trust, United Kingdom
Title : Stereotactic radiotherapy for wet age-related macular degeneration: year 4 results of a randomised, double-masked, sham-controlled trial
Tim Jackson, King’s College London, United Kingdom