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Up to: Inborn errors of metabolism · LCAT deficiency

Fish eye disease

Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterized clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency.

1 trial tagged with this condition →

This condition has no sub-types.