CNGB3-related retinopathy

CNGB3-related retinopathy is a rare eye condition that affects the retina, the light-sensitive tissue at the back of the eye. It occurs due to changes in both copies of the CNGB3 gene, which is important for normal retinal function. This condition is part of a group of inherited retinal disorders. Although detailed symptoms and progression are not fully detailed in the available sources, it is recognized as a genetic condition affecting vision.

Information about symptoms is currently limited for this condition.

CNGB3-related retinopathy is caused by biallelic variants in the CNGB3 gene. In people with this condition, mutations in both copies of the gene lead to misfunction in the retina, affecting vision.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.