The key to progress The homogeneity of RP and the lack of inventive step pose a serious problem for the development of new treatments (Marmor 1979, Greenwald 2009). It is a problem (Tsujikawa 2008). This is particularly troublesome as genetic counseling is the key to treating this disease, as there is currently no effective treatment.
Retinitis pigmentosa (RP). Retinitis pigmentosa is a hereditary eye disease found in more than 100,000 people in the United States. It can cause retinal degeneration and severe vision loss. It is a progressive disease that develops in childhood or adolescence, resulting in partial vision loss and night vision loss. It often causes serious vision impairment and sometimes even complete blindness. Learn more about Stargardt's disease with retinitis pigmentosa. Stargardt's disease is the most common form of hereditary adolescent macular degeneration and occurs every 8,000 to 10,000 people worldwide. It can lead to gentle loss of central vision. It usually develops in childhood or adolescence and loses the center of the field of view. Learn more about Stargardt disease
What should I do if I have been diagnosed with retinitis? Retinal pigmentary degeneration can not be cured, but there are several treatments that can delay the progression of the disease. These mainly include vitamin A supplements. Recent treatments include retinal implants and artificial retinas. Recent studies suggest that exposure to sunlight for long periods of time may increase the vision loss rate, so RP patients are advised to wear sunglasses outdoors. What kind of equipment is useful? For people with retinitis pigmentosa, which causes vision loss, the video loupe is useful. They can provide magnification and extra contrast and brightness to assist reading and other work. For people who have lost most or all of their sight, we recommend using screen reading software. Because retinitis pigmentosa usually begins in childhood, Braille is also a good solution when people are still learning how to read.