Retinitis pigmentosa associated with systemic disease (Q99753): Difference between revisions

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+August 2026Timestamp +2026-08-15T00:00:00Z
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Latest revision as of 16:25, 16 August 2026

This is an inherited, degenerative eye disease that causes severe vision impairment and often blindness. The progress of RP is not consistent. Some people will exhibit symptoms from infancy, others may not notice symptoms until later in life. Generally, the later the onset, the more rapid is the deterioration in sight. This diagnosis is associated with a disease that affects a number of organs and tissues, or affects the body as a whole.

Language	Label	Description	Also known as
default for all languages	ID_57089869
English	Retinitis pigmentosa associated with systemic disease	This is an inherited, degenerative eye disease that causes severe vision impairment and often blindness. The progress of RP is not consistent. Some people will exhibit symptoms from infancy, others may not notice symptoms until later in life. Generally, the later the onset, the more rapid is the deterioration in sight. This diagnosis is associated with a disease that affects a number of organs and tissues, or affects the body as a whole.