The term retinitis pigmentosa (RP) refers to a set of degenerative genetic diseases that gradually kill off the light-sensing cells (rods and cones) of the retina, eventually causing blindness. It is a relatively rare genetic disorder, affecting only 1 in 4,000 people. Retinitis pigmentosa can be difficult to adapt to without proper support. Although there is currently no cure for RP, regular visits with your eye care professional are important to monitor the progression of the disease, adapt to the condition, and become aware as new RP treatments are available.
Symptoms of Retinitis Pigmentosa
Although there are variations dictating how a person inherits and develops retinitis pigmentosa, this condition is usually characterized by the following symptoms:
- Poor and narrowing peripheral (side) vision.
- Difficulty seeing or driving in dimly-lit conditions. This is often called “night blindness.”
- As the disease progresses, vision may narrow to just a small, central vision field or “tunnel vision.”
- Difficulty discerning colors.
- Problems reading or doing intricate work due to deficiencies in the central field of vision, which often disappears first.
The progression of the disease can vary significantly depending on whether the condition is inherited as a dominant or recessive trait. Regular testing by your eye care professional is very important if you have RP for two reasons:
If you or a loved one suffers from any of these symptoms, please contact your eye care professional today for an appointment.