Late-onset retinal degeneration is a type of eye disorder that affects the retina, the light-sensitive layer of tissue at the back of the eye. It is characterized by progressive vision loss that begins in adulthood and can lead to blindness. Symptoms of late-onset retinal degeneration include blurred vision, difficulty seeing in dim light, and difficulty recognizing faces. Treatment options are limited and may include vitamin supplements, laser treatments, and surgery.

The symptoms of Late-onset retinal Degeneration can vary depending on the type of degeneration, but generally include:

-Decreased night vision

-Decreased peripheral vision

-Blurred vision

-Distorted vision

-Sensitivity to light

-Seeing spots or floaters

-Difficulty adapting to changes in light

-Difficulty recognizing colors

-Difficulty reading or seeing fine details

The causes of late-onset retinal degeneration are not fully understood. However, some potential causes include genetic mutations, environmental factors, and aging. Genetic mutations can cause changes in the proteins that make up the retina, leading to degeneration. Environmental factors such as exposure to ultraviolet light, smoking, and certain medications can also contribute to retinal degeneration. Finally, aging can cause the retina to become less efficient, leading to degeneration.

1. Low Vision Aids: Low vision aids such as magnifiers, telescopes, and closed-circuit television systems can help people with late-onset retinal degeneration to make the most of their remaining vision.

2. Surgery: Surgery may be an option for some people with late-onset retinal degeneration. This includes procedures such as vitrectomy, macular translocation, and retinal prosthesis.

3. Photodynamic Therapy: Photodynamic therapy (PDT) is a procedure that uses a light-activated drug to destroy abnormal blood vessels in the eye. This can help to slow the progression of late-onset retinal degeneration.

4. Nutritional Supplements: Taking certain nutritional supplements, such as lutein and zeaxanthin, may help to slow the progression of late-

1. Age: Late-onset retinal degeneration is more common in people over the age of 50.

2. Genetics: Certain genetic mutations can increase the risk of developing late-onset retinal degeneration.

3. Race: Late-onset retinal degeneration is more common in people of Asian descent.

4. Diabetes: People with diabetes are at an increased risk of developing late-onset retinal degeneration.

5. Smoking: Smoking increases the risk of developing late-onset retinal degeneration.

At this time, there is no cure for late-onset retinal degeneration. However, there are medications that can help slow the progression of the disease. These medications include anti-inflammatory drugs, antioxidants, and vitamins. Additionally, low-vision aids such as magnifiers and telescopic lenses can help improve vision.