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Retinitis Pigmentosa

Medically reviewed by Drugs.com. Last updated on Apr 2, 2024.

What is retinitis pigmentosa (RP)?

RP is a group of diseases that cause cells in the retina called rods to break down. Rods help you see at night and in low light. The retina is a thin layer of tissue that lines the back of your eye. The retina captures light and sends messages to your brain. The cell breakdown leads to vision loss that gets worse over time and may lead to blindness. Both eyes are affected, but one eye may have more severe vision loss than the other. RP is genetic (passed down through families). The genes may come from one or both sides of your family.

Eye Anatomy

What are the signs and symptoms of RP?

Signs and symptoms usually begin in childhood. You may develop any of the following:

How is RP diagnosed?

Your healthcare provider will ask about your symptoms and when they started. Tell your provider if you have any medical conditions or take any medicines. Tell your provider if you have a family history of RP. Family members other than your parents may have RP. You may also need any of the following:

How is RP treated?

RP cannot be cured. The goal is to slow the process so you keep as much vision as possible.

What can I do to manage RP?

Where can I find more information and support?

When should I seek immediate care?

When should I call my doctor?

Care Agreement

You have the right to help plan your care. Learn about your health condition and how it may be treated. Discuss treatment options with your healthcare providers to decide what care you want to receive. You always have the right to refuse treatment. The above information is an educational aid only. It is not intended as medical advice for individual conditions or treatments. Talk to your doctor, nurse or pharmacist before following any medical regimen to see if it is safe and effective for you.

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Treatment options

Symptoms and treatments

Further information

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