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Many research studies could not take place without the participation of people living with inherited sight loss.

Stickler syndrome is a genetic connective tissue disorder.

Refsum syndrome is an inherited metabolic condition, associated with elevated phytanic acid plasma levels, which impacts many body systems.

This edition of Look Forward includes the very latest news about an experimental therapy by Retina UK funded researchers, an article about one of our PhD students, a calendar of events in 2025, the usual research news round-up and lots more. Please take the time to complete our Sight Loss Survey, enclosed with this edition. You can find out more about the Survey.

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Cone-rod dystrophies are a group of inherited diseases that affect the photoreceptor (light sensing) cells that are responsible for capturing images from the visual field.

Choroideremia is a genetic condition that causes progressive vision loss, mostly in males.

Usher syndrome is an inherited condition that affects both hearing and vision.

Alstrom syndrome is an inherited condition which affects many body systems.

Achromatopsia is a rare hereditary vision disorder affecting approximately 1 in 30,000 newborn babies.

Familial Exudative Vitreoretinopathy (FEVR) is an inherited disorder that causes progressive vision loss.