Retinitis Pigmentosa Write for Us
Retinitis pigmentosa (RP) is a set of uncommon eye conditions that impair the retina, the layer of tissue at the back of the eye that is sensitive to light. RP causes the retina’s cells to deteriorate over time, impairing vision gradually.
RP is a hereditary condition that affects people from birth. Most people lose most of their vision; symptoms typically start in childhood.
There is no cure for RP. But vision assistance and rehabilitation (training) programs can help people with RP get the most out of their vision.
What are the Symptoms of Rheumatoid Arthritis?
The most common early symptom of RP is the loss of night vision – it usually starts in childhood. Parents may notice that children with RP struggle to move around in the dark or adjust to dim light.
Additionally, RP impairs peripheral (lateral) vision, making it difficult to see out of the corners of your eyes. Your field of vision gradually gets smaller until all you have is some central vision (also known as tunnel vision).
Some people with RP lose their sight more quickly than others. Eventually, most people with RP lose both their lateral and central vision.
Other Symptoms of RP Include:
Sensitivity to bright light
Loss of color vision
What causes RP?
RA is frequently brought on by gene modifications that govern the retinal cells. Children inherit these changed genes from their parents.
RP is linked to several genes and can be inherited in various ways. If you have RP, you may learn more about the dangers of transferring RP to your offspring by speaking with your doctor or a professional known as a genetic counselor.
Other genetic disorders like Usher syndrome can occasionally cause RP. Loss of hearing and vision are both effects of Usher syndrome.
RA can also be caused by certain medications, infections, or eye injury – but these causes are uncommon.
How will my Ophthalmologist Check RP?
As part of a thorough noninvasive eye exam, ophthalmologists can examine RP. The examination is quick and painless; after dilating your pupil with eye drops, the doctor will evaluate your eyes for RP and other eye issues. A visual field test is part of the exam to assess your side vision.
Other tests for RP include:
- Electroretinography (ERG). The ERG allows the ophthalmologist to check how well the retina responds to light.
- Optical coherence tomography (OCT). This test uses light waves to create a detailed picture of your retina.
- Fundus imaging (FAF). In this test, the ophthalmologist uses blue light to take a picture of your retina.
- Genetic analysis. Your doctor could advise genetic testing to learn more about the sort of RP they have. This can inform you of potential long-term changes in RP symptoms. What is the treatment for RP?
- There is no cure for RP, but low vision assistance and rehabilitation (training) programs can help people with RP get the most out of their vision.
Additionally, you can discuss vitamins and RP supplements with your ophthalmologist. A typical aspect of RP, visual loss, may be slowed down by vitamin A. However, taking too much vitamin A might result in liver issues; thus, discuss the advantages and disadvantages of this medication with your doctor. Supplements, including lutein and fish oil, may also reduce the loss of eyesight.
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