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Celebrate the life of your loved one, by donating in their memory and help us fund more research and support, now.
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Celebrate the life of your loved one, by donating in their memory and help us fund more research and support, now.
We can provide all the support your organisation needs to work with us; from ideas to practical support and materials. The Retina UK team will help your contribution be as fun and rewarding as possible.
X-linked inheritance means that the faulty gene is located on the X chromosome, the larger of the two sex chromosomes.
Biotechnology company ProQR has announced that its clinical trials of sepofarsen for Leber congenital amaurosis type 10 and ultevursen for USH2A-mediated retinitis pigmentosa will be wound down with immediate effect.
Prof Mariya Moosajee at Moorfields Eye Hospital has asked us to share the message below about the clinical trial she is running. This trial is for a treatment that targets a particular section of the USH2A gene.
As Luxturna reaches the clinic and other gene-specific therapies for inherited retinal disease get closer to the end of the development pipeline, it is becoming ever more important that affected families can access a genetic diagnosis, potentially opening up choices around treatment and clinical trial participation.
Disulfiram (Antabuse), FDA-approved for deterring alcohol, is in a phase 1 trial at the University of Washington to improve vision in retinitis pigmentosa.
Are you a parent or carer of a child or young person living with an inherited retinal dystrophy?
Stephen Goulden MBE attended the first British Retinitis Pigmentosa Society (BRPS) meeting in 1977. He describes his involvement with the charity and with inherited sight loss as follows:
For people living with inherited retinal conditions, finding others who understand can make a profound difference. In the South-West, volunteers Suzanne and Anne are helping to create those connections – offering support, understanding and a strong sense of community across a wide and largely rural area.