Flipping the switch on RP: SparingVision doses patients in their first in-human clinical trial for SPVN20
The latest research news from Retina UK.
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The latest research news from Retina UK.
SalioGen Developing Novel Gene Insertion Therapy for Stargardt disease.
The team have found the cause of disease in the first ever family tree drawn up at Moorfields Eye Hospital over 35 years ago, which had remained unsolved until now.
Researchers in the Netherlands are developing a “retina-on-a-chip” that mimics the key layers of the human retina, offering a powerful new way to study inherited retinal diseases (IRDs) and test potential treatments using human cells.
The following projects were being funded by Retina UK and have recently come to an end.
Choroideremia is a rare genetic condition resulting in progressive sight loss in men.
Autoimmune diseases are quite distinct from inherited retinal dystrophies.
This page explains the different types of genetic tests: diagnostic testing, predictive testing, carrier testing and research testing
Mini-retinas are essentially mini eyeballs in a dish. They contain all of the cell types in the human retina and we can perform many experiments on these to figure out the missing pieces in the puzzle.
Progress towards treatments for inherited retinal conditions continues to gather pace and there’s been lots going on in the last few months, with more and more approaches being explored. This round-up gives a flavour of the variety of developments, including plenty that are not specific to a particular genetic fault.