Retinitis Pigmentosa

Summarized by Plex Health
Last Updated: 04 May 2022
medpix case - retinitis pigmentosa "medpix case - retinitis pigmentosa", by Original Source: Herb Fechter, M.D., WRAMC Ophthalmology; Author: Aaron M Betts (Uniformed Services University); Approved By: Thomas P Ward (Uniformed Services University);. This photograph of the posterior pole shows the triad of bone spicule pigmentation, waxy pallor of the optic disc, and marked arteriolar attenuation....

Retinitis pigmentosa is a group of relevant eye disorders that cause progressive vision loss. In people with retinitis pigmentosa, vision loss happens as the light-sensing cells of the retina gradually degrade. The first sign of retinitis pigmentosa is usually a loss of evening vision, which comes to be obvious in childhood. In the adult years, lots of people with retinitis pigmentosa become legally blind. The most common form of syndromic retinitis pigmentosa is Usher disorder, which is identified by the combination of vision loss and hearing loss beginning early in life. However vision help and rehab programs can help people with RP make the most of their vision. Parents may observe that children with RP have trouble moving around in the dark or getting used to dark light. At some point, most individuals with RP lose their side vision and their central vision. Optometrist can look for RP as part of a detailed dilated eye examination. Retinitis pigmentosa is the name provided to a group of acquired eye diseases that affect the retina. Photoreceptor cells record and refine light aiding us to see. As these cells break down and die, patients experience progressive vision loss. Most forms of RP first cause the breakdown of pole cells. Evening loss of sight is somewhat like the experience normally spotted individuals encounter when entering a dark movie theater on a brilliant, sunny day. Nonetheless, patients with RP can not change well to dark and poorly lit environments.

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