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Autosomal recessive inheritance means that the faulty gene is on an autosome (any chromosome other than the sex chromosomes) and that both copies need to be faulty to cause sight loss

Are you affected by inherited sight loss? We are here to help. Retina UK is a national charity. We offer information and support to people affected by inherited sight loss to enable them to lead better lives today and fund medical research to accelerate the search for treatments for the future.

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X-linked inheritance means that the faulty gene is located on the X chromosome, the larger of the two sex chromosomes.

New Eye Care Support Pathway wins cross-sector backing for transforming the way people with care needs and sight loss are helped emotionally and practically.

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During our 50th Anniversary year, get involved in our annual Raffle! You could win 5 incredible prizes and support Retina UK at the same time.

Information for healthcare professionals: Genetic testing and counselling in inherited retinal disease

Join Lauren as she chats with Paula McGrath, Deputy CEO of Retina UK, about the 2025 Sight Loss Survey

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Different inherited sight loss conditions present noticeable symptoms at different times.

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Our monthly e-Newsletter featuring the latest updates from Retina UK. Subscribe now to receive these updates directly to your email.

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Emily Kearney is mum to four boys, aged four to 13, two of whom are living with an inherited sight loss condition.

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