IMPG1-related recessive retinopathy

IMPG1-related recessive retinopathy is a type of retinal disease that develops because of specific changes in the IMPG1 gene. These changes follow an autosomal recessive pattern, which means that people with the condition inherit two altered copies of the gene. The condition affects the retina, the light-sensitive tissue at the back of the eye. Information about the full range of symptoms and progression over time is currently limited for this condition.

Information about symptoms is currently limited for this condition.

This condition is caused by autosomal recessive variants in the IMPG1 gene. This means that changes in both copies of the gene lead to problems in the retina. Information about additional genetic or environmental risk factors is currently limited for this condition.

Information about treatment options and management for this condition is currently limited.

Information about the outlook and quality of life for people with this condition is currently limited.

Information about current research and future directions for this condition is currently limited.