Alstrom syndrome
Alstrom syndrome is an inherited condition which affects many body systems.
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Achromatopsia
Achromatopsia is a rare hereditary vision disorder affecting approximately 1 in 30,000 newborn babies.
Leber Congenital Amaurosis (LCA)
Leber Congenital Amaurosis (LCA) is a rare genetic eye disease that appears at birth or in the first few months of life.
Joining the research effort
Many research studies could not take place without the participation of people living with inherited sight loss.
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.
Bardet-Biedl syndrome (BBS)
Bardet-Biedl syndrome (BBS) is an inherited condition which impacts many parts of the body including the retina.
Retina UK Annual Conference 2024
The Retina UK Annual Conference will be held on Saturday 28 September. You can join the Conference in-person or online.
Stickler syndrome
Stickler syndrome is a genetic connective tissue disorder.
Retina UK Professionals’ Conference 2024
The Retina UK Professionals’ Conference is aimed at anyone who works with our community in a professional capacity.
X-linked retinoschisis (XLRS)
X-linked retinoschisis (XLRS) is an inherited condition that causes early loss of mainly central vision in males.