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We are currently funding a range of exciting projects and programmes, all of which aim to enhance our understanding of inherited sight loss, and inform the development of treatments for the estimated two million people affected worldwide.
Stargardt disease is the most common form of juvenile macular dystrophy (or inherited degeneration).
Bardet-Biedl syndrome (BBS) is an inherited condition which impacts many parts of the body including the retina.
Alstrom syndrome is an inherited condition which affects many body systems.
Could you take on an adventure of a lifetime for Retina UK and take part in the Sahara Desert Trek in November 2025?
James, who lives with retinitis pigmentosa, is running the TCS London Marathon in April 2025 to raise vital funds for Retina UK.
Gyrate atrophy of the choroid and retina, shortened to gyrate atrophy, is an inherited disorder of protein metabolism characterised by progressive vision loss.
Come together for Retina UK Day on Thursday, 10 October 2024 and help us raise awareness and funds for those who are living with inherited sight loss.
Many research studies could not take place without the participation of people living with inherited sight loss.
Join the Retina UK membership today! Anyone is welcome to join; whether you are living with a sight loss condition yourself, related to somebody who is, or if you are working as a sight loss professional.
