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New Device Offers Hope to People Blinded Due to Incurable Eye Disorders
Date:11/16/2013

NEW ORLEANS, Nov. 16, 2013 /PRNewswire-USNewswire/ -- Research presented today at the 117th Annual Meeting of the American Academy of Ophthalmology shows promising data about a device that helps people who have lost their vision due to a blinding genetic disease to recognize common objects. In the study, the researchers found when the objects' outlines had been enhanced, there was increased recognition. The device, called the Argus II, is the first FDA-approved retinal implant for adults with retinitis pigmentosa.

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Retinitis pigmentosa is a group of genetic disorders that affect the retina's ability to respond to light. The disease, which is inherited and affects about 1 in 4,000 Americans, causes slow loss of vision, beginning with decreased night vision and loss of peripheral vision and eventually leads to blindness.[i] Up to one-quarter of all patients with retinitis pigmentosa will become legally blind in both eyes.[ii] There is currently no cure for retinitis pigmentosa.

The Argus II retinal prosthesis is a system in which a miniature video camera is housed in the subject's glasses and sends information to a patient-worn video processing unit where the image captured by the camera is processed into instructions which are then transmitted wirelessly to a retinal implant fitted with 60 electrodes. These electrodes pulse to stimulate cells in the retina, transmitting visual information along the optic nerve to the brain, creating the perception of patterns of light.

In the study, eight patients wearing the retinal prosthesis were asked to identify white or metallic objects against a dark background, then were asked to identify the same objects with enhanced outlines. The tests were done in three ways – with the retinal pros
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SOURCE American Academy of Ophthalmology
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