Literature DB >> 18408503

Hereditary retinal disease.

Peter Goodwin1.   

Abstract

PURPOSE OF REVIEW: This article reports recent advances in the diagnosis, genetic analysis, and treatment of hereditary retinal disease. RECENT
FINDINGS: Clinicians and scientists continue to reveal the relationship between phenotype and genotype in hereditary retinal diseases. Persistent investigation and progressive technology are advancing the efficiency of mutation discovery. This technology is also leading to readily available genetic testing that aids clinicians in the diagnosis of these diseases. Functional genetic studies, and laboratory and human clinical trials are occurring that may lead to future treatment of these disorders.
SUMMARY: A literature review of the recent discoveries and potential treatments for retinitis pigmentosa, Leber's congenital amaurosis, X-linked retinoschisis, Best's disease, Stargardt's disease, and congenital stationary night blindness is presented, along with a guide for clinicians seeking genetic testing of patients.

Entities:  

Mesh:

Year:  2008        PMID: 18408503     DOI: 10.1097/ICU.0b013e3282fc27fc

Source DB:  PubMed          Journal:  Curr Opin Ophthalmol        ISSN: 1040-8738            Impact factor:   3.761


  21 in total

Review 1.  [Clinical manifestations of functional disturbances of the retinal pigment epithelium].

Authors:  M A Gamulescu; A B Renner; H Helbig
Journal:  Ophthalmologe       Date:  2009-04       Impact factor: 1.059

2.  Next generation sequencing in research and diagnostics of ocular birth defects.

Authors:  Gordana Raca; Craig Jackson; Berta Warman; Tom Bair; Lisa A Schimmenti
Journal:  Mol Genet Metab       Date:  2010-03-15       Impact factor: 4.797

3.  Surgical treatment for complications of congenital retinoschisis.

Authors:  Jiang You
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2011-06-14

4.  G protein signaling in the retina and beyond: the Cogan lecture.

Authors:  Kirill A Martemyanov
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-12-15       Impact factor: 4.799

5.  Identification of a mutation in CNNM4 by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1.

Authors:  Sisi Li; Quansheng Xi; Xiaoyu Zhang; Dong Yu; Lin Li; Zhenyang Jiang; Qiuyun Chen; Qing K Wang; Elias I Traboulsi
Journal:  Mol Genet Genomics       Date:  2018-01-10       Impact factor: 3.291

6.  Long-term RNA interference gene therapy in a dominant retinitis pigmentosa mouse model.

Authors:  Li Jiang; Houbin Zhang; Alexander M Dizhoor; Shannon E Boye; William W Hauswirth; Jeanne M Frederick; Wolfgang Baehr
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-31       Impact factor: 11.205

7.  Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa.

Authors:  Stephan Züchner; Julia Dallman; Rong Wen; Gary Beecham; Adam Naj; Amjad Farooq; Martin A Kohli; Patrice L Whitehead; William Hulme; Ioanna Konidari; Yvonne J K Edwards; Guiqing Cai; Inga Peter; David Seo; Joseph D Buxbaum; Jonathan L Haines; Susan Blanton; Juan Young; Eduardo Alfonso; Jeffery M Vance; Byron L Lam; Margaret A Peričak-Vance
Journal:  Am J Hum Genet       Date:  2011-02-03       Impact factor: 11.025

Review 8.  Ciliary ectosomes: transmissions from the cell's antenna.

Authors:  Christopher R Wood; Joel L Rosenbaum
Journal:  Trends Cell Biol       Date:  2015-01-21       Impact factor: 20.808

9.  Expression of rod-derived cone viability factor: dual role of CRX in regulating promoter activity and cell-type specificity.

Authors:  Sophie Lambard; Sacha Reichman; Cynthia Berlinicke; Marie-Laure Niepon; Olivier Goureau; José-Alain Sahel; Thierry Léveillard; Donald J Zack
Journal:  PLoS One       Date:  2010-10-07       Impact factor: 3.240

10.  Statistical genetic approaches for mapping ophthalmic trait and disease genes.

Authors:  Janet Sinsheimer
Journal:  Am J Ophthalmol       Date:  2009-08       Impact factor: 5.258

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