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Rare syndromes

These very rare syndromes (NARP, Bassen-Kornweig, PXE, Norrie) affect the eyes as well as other parts of the body.

A group of supporters taking on 5K A Day In May.

5K A Day In May 2025

May is National Walking Month! Are you ready to join #TeamRetinaUK in May for our daily 5K challenge? Your support will allow us to continue supporting those who are living with inherited sight loss.

Cataracts and Macular Oedema

Cataracts and macular oedema are both associated with inherited sight loss and may respond to treatment.

Familial Exudative Vitreoretinopathy (FEVR)

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

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.

Doyne honeycomb dystrophy

Doyne honeycomb dystrophy is an inherited disorder which causes progressive sight loss.

Retina UK knowledge-base Central areolar choroidal dystrophy

Central areolar choroidal dystrophy (CACD)

Central Areolar Choroidal Dystrophy (CACD) is a rare inherited condition that affects the macula, the small area in the middle of the retina that is primarily responsible for our central vision.