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Retina UK Knowledge-base: Cone-rod dystrophy

Cone-rod dystrophy

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.

Retina UK Knowledge-base: Achromatopsia

Achromatopsia

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

Retina UK Knowledge-base: X-linked retinoschisis

X-linked retinoschisis (XLRS)

X-linked retinoschisis (XLRS) is an inherited condition that causes early loss of mainly central vision in males.

Members of the Berkshire local peer support group sitting around a table

Local peer support groups

Our Retina UK Peer Support Group network offers information and support via regular meetings both online or in-person.

Retina UK Knowledge-base: Usher syndrome

Usher syndrome

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

Retina UK Knowledge-base: Refsum syndrome

Refsum syndrome

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