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Pattern dystrophy is an umbrella term for a group of retinal conditions. It is characterized by various patterns of pigment deposition within the macula.

We are currently funding a range of exciting projects and programmes, all of which aim to enhance our understanding of inherited sight loss, and inform the development of treatments for the estimated two million people affected worldwide.

Bardet-Biedl syndrome (BBS) is an inherited condition which impacts many parts of the body including the retina.

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.

The content on this site will have answered some of your queries about inherited sight loss and associated syndromes, but everyone’s circumstances are different and you may have further questions.

Leber Congenital Amaurosis (LCA) is a rare genetic eye disease that appears at birth or in the first few months of life.

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

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Are you looking for a thrill with a view? Could you take on a skydive for Retina UK this summer? Join us at various airfields around the UK this July.

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