Stargardt Disease
Stargardt Disease is an eye condition that primarily affects the retina, the part of the eye responsible for vision. It is usually inherited and leads to progressive vision loss, particularly in the central vision, making it difficult to see fine details or read. This disease typically begins in childhood or early adulthood, and while it is not curable, some people may retain peripheral vision. Researchers are exploring various treatments and potential therapies to slow its progression or restore vision. Early diagnosis and support can help those affected manage their condition better.
Additional Insights
-
Stargardt disease is a genetic eye disorder that primarily affects young people, leading to progressive vision loss. It is caused by mutations in genes responsible for the function of photoreceptor cells in the retina, which detect light and enable vision. Symptoms typically include difficulty seeing in low light and a gradual loss of central vision, impacting activities like reading and recognizing faces. While there is currently no cure, research continues into potential therapies, including gene treatment and retinal implants, aiming to slow the progression of the disease and improve quality of life for those affected.