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Retina UK Knowledge-base: Gyrate atrophy

Gyrate atrophy of the choroid and retina

Gyrate atrophy of the choroid and retina, shortened to gyrate atrophy, is an inherited disorder of protein metabolism characterised by progressive vision loss.

Retina UK Knowledge-base: Usher syndrome

Usher syndrome

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

Retina UK Knowledge-base: Stargardt disease

Stargardt disease

Stargardt disease is the most common form of juvenile macular dystrophy (or inherited degeneration).

Knowledge-base, Bardet-biedl syndrome

Bardet-Biedl syndrome (BBS)

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

Retina UK Knowledge-base: Achromatopsia

Achromatopsia

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