Literature DB >> 17065520

Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degeneration.

Amir A Azari1, Tomas S Aleman, Artur V Cideciyan, Sharon B Schwartz, Elizabeth A M Windsor, Alexander Sumaroka, Andy Y Cheung, Janet D Steinberg, Alejandro J Roman, Edwin M Stone, Val C Sheffield, Samuel G Jacobson.   

Abstract

PURPOSE: To define the retinal phenotype in patients with the Bardet-Biedl syndrome and mutations in the BBS1 gene.
METHODS: Ten patients (age range, 16-48 years), representing eight pedigrees, with BBS1 gene mutations were studied clinically and with kinetic perimetry, chromatic static perimetry, electroretinography (ERG), and optical coherence tomography.
RESULTS: Of the 10 patients, 8 were M390R homozygotes and 2 were compound heterozygotes with one allele also M390R. A spectrum of retinal disease expression was present. The mildest disease was a subtle maculopathy with relatively limited peripheral retinal dysfunction. Moderate disease showed retina-wide rod > cone dysfunction, and often there was a negative ERG waveform. More severe disease expression had different patterns: either loss of central function but retained abnormal peripheral function or a retained small central island of impaired function only. Moderate and severe disease showed loss of retinal and photoreceptor layer thickness across wide expanses of retina. Severity differed in family members and was independent of age. In addition, severity was not explained by genotype at a recently reported BBS epistatic gene, MGC1203.
CONCLUSIONS: The cardinal feature of retinal degeneration in BBS1 can show a wide spectrum of disease expression.

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Year:  2006        PMID: 17065520     DOI: 10.1167/iovs.06-0517

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  24 in total

1.  Retinal morphology in patients with BBS1 and BBS10 related Bardet-Biedl Syndrome evaluated by Fourier-domain optical coherence tomography.

Authors:  Christina Gerth; Robert J Zawadzki; John S Werner; Elise Héon
Journal:  Vision Res       Date:  2007-11-05       Impact factor: 1.886

2.  Combining fetal sonography with genetic and allele pathogenicity studies to secure a neonatal diagnosis of Bardet-Biedl syndrome.

Authors:  E Ashkinadze; T Rosen; S S Brooks; N Katsanis; E E Davis
Journal:  Clin Genet       Date:  2012-10-14       Impact factor: 4.438

3.  Peripheral Gene Therapeutic Rescue of an Olfactory Ciliopathy Restores Sensory Input, Axonal Pathfinding, and Odor-Guided Behavior.

Authors:  Warren W Green; Cedric R Uytingco; Kirill Ukhanov; Zachary Kolb; Jordan Moretta; Jeremy C McIntyre; Jeffrey R Martens
Journal:  J Neurosci       Date:  2018-07-30       Impact factor: 6.167

4.  Gene therapy prevents photoreceptor death and preserves retinal function in a Bardet-Biedl syndrome mouse model.

Authors:  David L Simons; Sanford L Boye; William W Hauswirth; Samuel M Wu
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-28       Impact factor: 11.205

Review 5.  Genetic characterization and disease mechanism of retinitis pigmentosa; current scenario.

Authors:  Muhammad Umar Ali; Muhammad Saif Ur Rahman; Jiang Cao; Ping Xi Yuan
Journal:  3 Biotech       Date:  2017-07-18       Impact factor: 2.406

6.  Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations.

Authors:  Wei Chieh Huang; Artur V Cideciyan; Alejandro J Roman; Alexander Sumaroka; Rebecca Sheplock; Sharon B Schwartz; Edwin M Stone; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-03-20       Impact factor: 4.799

7.  Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia.

Authors:  Alok S Shah; Sara L Farmen; Thomas O Moninger; Thomas R Businga; Michael P Andrews; Kevin Bugge; Charles C Searby; Darryl Nishimura; Kim A Brogden; Joel N Kline; Val C Sheffield; Michael J Welsh
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-25       Impact factor: 11.205

8.  Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.

Authors:  Tomas S Aleman; Artur V Cideciyan; Alexander Sumaroka; Sharon B Schwartz; Alejandro J Roman; Elizabeth A M Windsor; Janet D Steinberg; Kari Branham; Mohammad Othman; Anand Swaroop; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-10       Impact factor: 4.799

9.  A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity.

Authors:  Roger E Davis; Ruth E Swiderski; Kamal Rahmouni; Darryl Y Nishimura; Robert F Mullins; Khristofor Agassandian; Alisdair R Philp; Charles C Searby; Michael P Andrews; Stewart Thompson; Christopher J Berry; Daniel R Thedens; Baoli Yang; Robert M Weiss; Martin D Cassell; Edwin M Stone; Val C Sheffield
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-21       Impact factor: 11.205

10.  Harmonin in the murine retina and the retinal phenotypes of Ush1c-mutant mice and human USH1C.

Authors:  David S Williams; Tomas S Aleman; Concepción Lillo; Vanda S Lopes; Louise C Hughes; Edwin M Stone; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-03-25       Impact factor: 4.799

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