
Bardet-Biedl syndrome (BBS)
Bardet-Biedl syndrome (BBS) is an inherited condition which impacts many parts of the body including the retina.
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Bardet-Biedl syndrome (BBS) is an inherited condition which impacts many parts of the body including the retina.
Achromatopsia is a rare hereditary vision disorder affecting approximately 1 in 30,000 newborn babies.
Pattern dystrophy is an umbrella term for a group of retinal conditions. It is characterized by various patterns of pigment deposition within the macula.
Since we were founded in 1976, we have invested more than £17 million into some of the most pioneering medical research - because of amazing supporters like you.
Gyrate atrophy of the choroid and retina, shortened to gyrate atrophy, is an inherited disorder of protein metabolism characterised by progressive vision loss.
May is National Walking Month! Are you ready to join #TeamRetinaUK in May for our daily 5K challenge? Your support will allow us to continue supporting those who are living with inherited sight loss.
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Is 2024 the year that you join #TeamRetinaUK & take on the Sheffield 10K?
Charles Bonnet syndrome (CBS) causes people who have lost a lot of sight to see things that aren’t real (hallucinations).
Do you want to take part in the world-famous TCS London Marathon, from the comfort of your own city? Take part virtually on race day and join #TeamRetinaUK in 2025!