Bardet-Biedl syndrome (BBS)
Bardet-Biedl syndrome (BBS) is an inherited condition which impacts many parts of the body including the retina.
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Bardet-Biedl syndrome (BBS) is an inherited condition which impacts many parts of the body including the retina.
Stickler syndrome is a genetic connective tissue disorder.
Many research studies could not take place without the participation of people living with inherited sight loss.
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.
As well as many of the well known races, we also have places available in hundreds of local runs. Wherever you live, you can run as part of #TeamRetinaUK!
These very rare syndromes (NARP, Bassen-Kornweig, PXE, Norrie) affect the eyes as well as other parts of the body.
Pattern dystrophy is an umbrella term for a group of retinal conditions. It is characterized by various patterns of pigment deposition within the macula.
X-linked retinoschisis (XLRS) is an inherited condition that causes early loss of mainly central vision in males.
Gyrate atrophy of the choroid and retina, shortened to gyrate atrophy, is an inherited disorder of protein metabolism characterised by progressive vision loss.
Our Retina UK Peer Support Group network offers information and support via regular meetings both online or in-person.