Stickler syndrome
Stickler syndrome is a genetic connective tissue disorder.
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Joining the research effort
Many research studies could not take place without the participation of people living with inherited sight loss.
Choroideremia
Choroideremia is a genetic condition that causes progressive vision loss, mostly in males.
Retinitis pigmentosa
Retinitis pigmentosa (RP) is an inherited eye condition that affects the photoreceptor cells responsible for capturing images from the visual field.
Refsum syndrome
Refsum syndrome is an inherited metabolic condition, associated with elevated phytanic acid plasma levels, which impacts many body systems.
Alstrom syndrome
Alstrom syndrome is an inherited condition which affects many body systems.
Achromatopsia
Achromatopsia is a rare hereditary vision disorder affecting approximately 1 in 30,000 newborn babies.
Best disease
Best disease, also known as Best vitelliform macular dystrophy (BVMD), is is an inherited eye condition associated with progressive degeneration of the macula and is a form of juvenile macular dystrophy.
X-linked retinoschisis (XLRS)
X-linked retinoschisis (XLRS) is an inherited condition that causes early loss of mainly central vision in males.
TCS London Marathon MyWay 2026 (Virtual Event)
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!