Retinitis Pigmentosa is a hereditary eye condition affecting the retina. Patients suffer from a form of "tunnel vision" and night blindness most commonly. This category includes both informational sites and organizations.
Self-help group fighting blindness in the UK through direct research. Information on research, location of local groups and FAQs. Formatted in easy-read colour schemes.
Article by Anthony de Beus, MD, PhD
Details and links to articles and resources.
Basic information on cause, symptoms, examination, treatment and prognosis.
A voluntary organization that provides scientific research, information and support to people and families affected by retinal degenerative diseases. Find details about grants, events, and how you can help.
Voluntary charitable umbrella association of 34 national societies each of whose aim is to find a cure for RP and other retinal diseases.
Personal page written by the child of an RP patient. Includes a description of the development of the condition.
Gives general information and research details on RP.
Information on diagnosis, causes and treatment.
Discussion group where people with Retinitis Pigmentosa gather for friendship and support.
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