Gene editing has revolutionized the possibilities for treating numerous inherited disorders, but its potential for retinal diseases like autosomal dominant retinitis pigmentosa (adRP) stands...
Bardet-Biedl Syndrome (BBS) is a rare genetic condition characterized by a range of symptoms, including vision loss that often progresses to blindness. As the...
Leber Congenital Amaurosis (LCA) is a rare, inherited eye disorder that leads to severe vision loss at birth or in early infancy. Traditional treatments...
Pathogenic myopia, a severe form of nearsightedness, poses significant challenges to individuals worldwide, often leading to irreversible vision impairment and increasing the risk of...
Leber Hereditary Optic Neuropathy (LHON) is a devastating mitochondrial disorder that leads to acute or subacute loss of central vision, primarily affecting young adults....