Condition
Retinitis Pigmentosa
Ophthalmology
Overview
Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Retinitis Pigmentosa
- Topic type
- Condition
- Category
- Ophthalmology
- MeSH classification
- C11.270.684|C11.768.585.658.500|C16.320.290.684
Preparing for an appointment about Retinitis Pigmentosa
If you are speaking with a healthcare professional about Retinitis Pigmentosa, it can help to prepare a few details in advance.
- Write down your symptoms and when they started.
- Bring details of any medicines, supplements or previous treatments.
- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
Finding care related to Retinitis Pigmentosa
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.