Stargardt disease is a rare genetic eye condition that is caused due to the build-up of fatty materials on the macula. The initial symptom of Stargardt disease is the loss of central vision. Still, peripheral vision is unaffected, with difficulty in color perception and adapting to bright to dark or from dark to bright environments.
Stargardt Disease - Symptoms, Diagnosis, and Management
Stargardt disease is a type of juvenile macular degeneration disorder resulting in the loss of vision in children and young adults.
