Stargardt’s disease is an hereditary form of macular degeneration characterized by central vision loss but preserved peripheral vision, caused by mutations in the ABCA4 gene. Oral therapy has proven successful

Stargardt disease is a genetic condition in which fatty material accumulates in the macula of the retina, the portion responsible for central vision. Vision loss typically begins in childhood or

This 36-year-old patient suffers from Stargardt disease and has central vision of 20/400 in each eye. Fundus autofluorescence scans show dark areas indicative of retinal pigment epithelium atrophy (yellow arrows).

Stargardt disease is a genetic condition which leads to central vision becoming clouded and distorted, making it the most prevalent form of hereditary macular dystrophy. Mutationss in the ABCA4 gene

Stargardt disease is caused by genetic mutations to the ABCA4 gene that lead to lipofuscin accumulation within retinal cells, leading to loss of central vision. Stargardt Macular Degeneration currently does

Stargardt disease is an inherited eye condition that damages the retina (light-sensitive tissue lining the inside of your eyes), resulting in central vision loss but maintaining peripheral vision. Sequence variants

Stargardt disease is an autosomal recessive juvenile macular degeneration disorder characterized by yellowish round flecks in the macula, usually due to mutations of ABCA4 gene. Over time, vision deteriorates until

Stargardt disease is an inherited retinal condition caused by mutations in several genes; symptoms generally manifest themselves during childhood or adolescence. Ascidian Therapeutics’ lead program targets ABCA4-associated retinopathies, such as

Stargardt eye disease, also known as Stargardt degeneration, usually manifests before age 20 and causes progressive loss of central vision and color perception. It’s usually an irreversible condition. LBS-008, an

Stargardt disease is an inherited disorder that attacks the macula of the retina and leads to loss of central vision as well as distortion of color perception. This condition is