Retinitis Pigmentosa

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Humans, have developed numerous diseases during our time here on Earth. In order to stay healthy doctors have had to establish treatments able to heal the sick, with modern equipment doctors are able to do just that. Machines are helpful to a certain extent only when the source of a disease is identified can a doctor possibly begin to examine it and eventually proceed towards a solution. While many cures have been developed many conditions still exist currently incurable like Retinitis Pigmentosa. The process for curing a disease can be long and difficult. In order to develop an antidote doctors must find the cause of a disease, conduct research and determine an approved course to take in order to cure it.
First labeled as Retinitis Pigmentosa by Doctor Donders in 1857, Retinitis Pigmentosa (RP) is a condition which causes the rods and cones in a patient’s eye to degenerate. Cones are responsible for allowing people to see during the day and in color. Rods allow people to see in low light environments. RP is most commonly inherited by one’s parents, of which both carry the recessive gene responsible for RP, although some isolated cases occur. The first signs of RP is impaired night vision often observed during childhood followed by the narrowing of peripheral vision. In mild cases tunnel vision doesn’t develop until the fifth or sixth decade (Willacy). Patients with RP are commonly diagnosed in their teens. In order to diagnose RP the patient must go through a series of examinations. The First is an initial assessment followed by a visual acuity test, a common test evaluates the sharpness of the retinal focus within the eye. Followed by a visual field assessment to test a patient’s peripheral vision. Both these tests...

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