Genome-wide studies, to identify new genes linked to glaucoma, are essential to better understand the mechanisms underlying the disease and ameliorate the treatments for patients. This is the first step to achieve the optimal therapy through a personalized therapy.
Researchers have recently used gene therapy in a study to successfully restore vision in mice by manipulating eye cells in the retina to recapture youthful gene function. It is the first successful attempt to reverse glaucoma-induced vision loss rather than merely stem its progression. The future goal will be fixing the biologic defect in patients with glaucoma.
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