What is genetic disease sra3?

SRA3, or "Syndromic Retinal Atrophy 3," is a genetic disorder characterized by progressive vision loss due to retinal degeneration. It is associated with mutations in specific genes that affect the structure and function of retinal cells. The condition is often inherited in an autosomal recessive pattern, meaning both copies of the gene in an individual must be mutated for the disease to manifest. Symptoms typically appear in childhood or adolescence and can lead to significant visual impairment over time.