Retinitis pigmentosa
Retinitis pigmentosa, or RP, is a genetic eye condition. Generally, night blindness precedes tunnel vision by years or even decades. Many people with RP do not become legally blind until their 40s or 50s and retain some sight all their life. Others go completely blind from RP, in some cases as early as childhood. Progression of RP is different in each case.
Related Topics:
Eye - Night blindness - Tunnel vision - Blind
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RP is a group of inherited disorders in which abnormalities of the photoreceptors (rods and cones) or the retinal pigment epithelium (RPE) of the retina lead to progressive visual loss. Affected individuals first experience defective dark adaptation or nyctalopia (night blindness), followed by constriction of the peripheral visual field and, eventually, loss of central vision late in the course of the disease.
Related Topics:
Photoreceptors - Rod - Cone - Retina - Nyctalopia - Peripheral visual field
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~ Table of Content ~
| ► | Introduction |
| ► | Signs |
| ► | Diagnosis |
| ► | Treatment |
| ► | External links |
| ► | Sources |
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