MERTK-related retinopathy

MERTK-related retinopathy is an inherited eye condition. It is known as a retinopathy because it primarily affects the retina, which is the light-sensitive layer at the back of the eye. This condition is caused by bi-allelic variants in the MERTK gene, meaning that changes in both copies of the gene contribute to the development of the disease. This condition is genetic in nature, and it affects the process by which the retina functions. The role of the MERTK gene is important in maintaining the health of the retina, and when both copies of this gene have variants, it leads to problems in the retinal cells. This summary gives a basic overview of the condition based on the available information.

Information about symptoms is currently limited for this condition.

MERTK-related retinopathy is caused by bi-allelic variants in the MERTK gene. This means that each affected person has variations in both copies of the gene, leading to impairment in the normal function of the retina. The genetic changes affect the way retinal cells work and can lead to vision problems associated with this retinopathy.

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.