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Posts Tagged ‘Leber congenital amaurosis (LCA)’

Utilizing Genetics & Nanoparticles to Treat Inherited Retinal Diseases

Many eye diseases, such as Retinitis Pigmentosa, Leber Congenital Amaurosis (LCA) and Stargardt Disease, have a genetic basis. Researchers are studying these and other inherited retinal diseases in order to identify the genes responsible and to use this information to develop genetic tests and treatments. Research projects at the National Eye Institute, Oregon State University […]

Fixing What’s Broken

Spend enough time around eye doctors or in my case, reading about eye and vision research and you will learn that the eyes are the front of the brain. While the eyes are taking in the visuals, it is the brain that is interpreting them. Most of time, things work correctly, and people see what […]

Gene Therapy for Leber Congenital Amaurosis

Leber Congenital Amaurosis (LCA) is a genetic eye disease that affects the retina. It is caused by a mutation in 14 genes that have a role in the development of the retina. Visual impairment starts in infancy and for the most part remains stable, though it can get worse over time. Those with LCA experience […]

Cutting the Fat & Turning Back the Clock

During the coronavirus lockdown, many people used this time to exercise more. As a result, their clothes aren’t as tight and they felt better. The bad thing about the lockdown is that it led to a lot of shortages, like toilet paper. Too bad we can’t turn back the clock to February 2020 and stock […]