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.
Face your fears and support Retina UK with a charity skydive this summer!
Gyrate atrophy of the choroid and retina, shortened to gyrate atrophy, is an inherited disorder of protein metabolism characterised by progressive vision loss.
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The Retina UK Professionals’ Conference is aimed at anyone who works with our community in a professional capacity.
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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 2026!
Our new Retina UK online auction is now live! Get bidding to win fantastic prizes and support those living with inherited sight loss.