Retinitis pigmentosa 3

Common Name(s)

Retinitis pigmentosa 3

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Retinitis pigmentosa 3" 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 3" returned 12 free, full-text research articles on human participants. First 3 results:

An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3.
 

Author(s): Ahmed Bouhouche, Ali Benomar, Leila Errguig, Lamiae Lachhab, Naima Bouslam, Jehanne Aasfara, Sanaa Sefiani, Layachi Chabraoui, Elmostafa El Fahime, Abdeljalil El Quessar, Mohamed Jiddane, Mohamed Yahyaoui

Journal:

 

Single-gene disorders related to ischemic stroke seem to be an important cause of stroke in young patients without known risk factors. To identify new genes responsible of such diseases, we studied a consanguineous Moroccan family with three affected individuals displaying hereditary ...

Last Updated: 7 May 2012

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ω-3 intake and visual acuity in patients with retinitis pigmentosa receiving vitamin A.
 

Author(s): Eliot L Berson, Bernard Rosner, Michael A Sandberg, Carol Weigel-DiFranco, Walter C Willett

Journal: Arch. Ophthalmol.. 2012 Jun;130(6):707-11.

 

To evaluate whether a diet high in long chain ω-3 fatty acids can slow the rate of visual acuity loss among patients with retinitis pigmentosa receiving vitamin A palmitate.

Last Updated: 14 Sep 2012

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Phenotypic characterization of 3 families with autosomal dominant retinitis pigmentosa due to mutations in KLHL7.
 

Author(s): Yuquan Wen, Kirsten G Locke, Martin Klein, Sara J Bowne, Lori S Sullivan, Joseph W Ray, Stephen P Daiger, David G Birch, Dianna K Hughbanks-Wheaton

Journal: Arch. Ophthalmol.. 2011 Nov;129(11):1475-82.

 

To characterize the visual phenotype caused by mutations in the BTB-Kelch protein, KLHL7, responsible for the RP42 form of autosomal dominant retinitis pigmentosa (RP).

Last Updated: 15 Nov 2011

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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 3" returned 1 free, full-text review articles on human participants. First 3 results:

Insights into X-linked retinitis pigmentosa type 3, allied diseases and underlying pathomechanisms.
 

Author(s): Paulo A Ferreira

Journal: Hum. Mol. Genet.. 2005 Oct;14 Spec No. 2():R259-67.

 

In the past decade, we have witnessed great advances in the identification of genes underlying numerous neurodegenerative diseases and the stark complexity determining genotype-phenotype relationships that lead to the impairment, and ultimately, premature death of neurons. However, ...

Last Updated: 24 Oct 2005

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Retinal Imaging of Subjects Implanted With Ciliary Neurotrophic Factor (CNTF)-Releasing Encapsulated Cell Implant for Early-stage Retinitis Pigmentosa
 

Status: Recruiting

Condition Summary: Retinitis Pigmentosa; Usher Syndrome Type 2; Usher Syndrome Type 3

 

Last Updated: 27 Feb 2014

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