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Podcast: What is the UKIRDC and why does it exist?

With a significant proportion of inherited retinal conditions being caused by unidentified genetic faults, and many families unable to get clear results from genetic tests in clinic, the project set out to solve previously undiagnosable cases and discover more of the genes and mutations that are associated with sight loss.

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Information and support services

Whether you are looking for practical information or emotional support, online, by phone or face-to-face, we’re here to help.

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Therapy development updates

There are many ongoing clinical and laboratory studies around the world, exploring innovative approaches to treating inherited sight loss.

About Unlock Genetics

The aim of the site is to increase the level of awareness and understanding of genetic testing and genetic counselling among people living with inherited retinal dystrophies, empowering them to make fully informed decisions about their lives, healthcare and family planning.