Retinitis Pigmentosa 9

Common Name(s)

Retinitis Pigmentosa 9

Autosomal dominant retinitis pigmentosa (ADRP) is characterized by a typical fundus appearance, narrowed retinal vessels, and changes in the electrophysiological responses of the eye. Early signs are night blindness and constriction of the visual fields with a variable ages of onset (summary by {4:Jay et al., 1992}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Retinitis Pigmentosa 9" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Retinitis Pigmentosa 9" returned 1 free, full-text research articles on human participants. First 3 results:

Genetic mapping of the human amphiphysin gene (AMPH) at 7p14-p13 excludes its involvement in retinitis pigmentosa 9 or dominant cystoid macular dystrophy.
 

Author(s): R Yamamoto, X Li, U Francke, M W Kilimann

Journal: Am. J. Hum. Genet.. 1995 Oct;57(4):970-2.

 

Last Updated: 3 Nov 1995

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Retinitis Pigmentosa 9" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

The Effect of Oral Administration of 9-cis β Carotene Rich Powder of the Alga Dunaliella Bardawil
 

Status: Recruiting

Condition Summary: Retinitis Pigmentosa

 

Last Updated: 1 Jan 2017

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