PROM1-related dominant retinopathy

PROM1-related dominant retinopathy is a condition that affects the retina, the light-sensitive tissue at the back of the eye. It is caused by changes in the PROM1 gene, where a single altered copy of the gene can lead to the condition. Because the change is autosomal dominant, people with this variant have the possibility of developing retinopathy due to the altered gene. This summary is based on limited available information about the condition.

Information about symptoms is currently limited for this condition.

PROM1-related dominant retinopathy is caused by an autosomal dominant variant in the PROM1 gene. This means that only one altered copy of the gene may lead to the development of the condition. Detailed information about other genetic or environmental risk factors is currently limited.

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.