Leber Congenital Amaurosis

Leber Congenital Amaurosis (LCA) is a rare genetic eye disorder that affects vision from birth or early childhood. It results from mutations in genes that are essential for the function of retinal cells, which capture light and send visual signals to the brain. People with LCA often experience severe vision loss or blindness, as they may have trouble seeing shapes or colors. Early diagnosis and support can help manage the condition, and advancements in gene therapy are being explored as potential treatments to restore some degree of vision in affected individuals.