ATSN-201 is a subretinal candidate that delivers the RS1 gene in the eye to potentially achieve a functional cure for ...

Two gene mutations that trigger a retinal disease that causes blindness in one in 5,000 males have been mapped, leading to the potential for new therapeutic treatments. Researchers at the ...

There are two types of retinal detachments associated with retinoschisis: a localized and relatively stable form with outer retinal holes only; and a symptomatic, rapidly progressive detachment ...

Researchers from The University of Manchester undertook a structural analysis of X-linked Retinoschisis (XLRS), a genetic disease leading to a type of macular degeneration in which the inner layers of ...

But the very sport could make Pierce's vision worse. He was diagnosed with X-linked retinoschisis. Simply put, Pierce is slowly going blind. He's already lost vision in his right eye. "He does ...

In recent years, advances in molecular genetics have impacted the understanding and the classification of hereditary retinal and optic nerve disease perhaps more than any other group of eye ...

including ocular (X-linked retinoschisis pigmentosa, choroideremia, Leber hereditary optic neuropathy), neurological (Alzheimer’s disease, Parkinson’s disease, Huntington’s disease ...

The company develops ABO-503 for the treatment of X-linked retinoschisis; ABO-504 for the treatment of stargardt disease; and ABO-505 for the treatment of autosomal dominant optic atrophy.