Stargardt's macular degeneration, also called juvenile macular degeneration, is an inherited disease which affects one in 10,000 people. This condition results from a defect in the ABCR gene, which is responsible for coding for a protein that removes all-trans-retinaldehyde, a vision byproduct, from retinal rods and cones. Rods and cones are supported by retinal-pigmented epithelium (RPE), a layer of cells near the retina. The accumulation of toxic pigments, or lipofuscin...Read More