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Bardet-Biedl syndrome-7 ( BBS7 ) shows treatment potential and a cone-rod dystrophy phenotype that recapitulates the non-human primate model.

Authors :
Aleman TS
O'Neil EC
O'Connor K
Jiang YY
Aleman IA
Bennett J
Morgan JIW
Toussaint BW
Source :
Ophthalmic genetics [Ophthalmic Genet] 2021 Jun; Vol. 42 (3), pp. 252-265. Date of Electronic Publication: 2021 Mar 17.
Publication Year :
2021

Abstract

Purpose : To provide a detailed ophthalmic phenotype of two male patients with Bardet-Biedl Syndrome (BBS) due to mutations in the BBS7 gene Methods : Two brothers ages 26 (Patient 1, P1) and 23 (P2) underwent comprehensive ophthalmic evaluations over three years. Visual function was assessed with full-field electroretinograms (ffERGs), kinetic and chromatic perimetry, multimodal imaging with spectral domain optical coherence tomography (SD-OCT), fundus autofluorescence (FAF) with short- (SW) and near-infrared (NIR) excitation lights and adaptive optics scanning light ophthalmoscopy (AOSLO). Results : Both siblings had a history of obesity and postaxial polydactyly; P2 had diagnoses of type 1 Diabetes Mellitus, Addison's disease, high-functioning autism-spectrum disorder and -12D myopia. Visual acuities were better than 20/30. Kinetic fields were moderately constricted. Cone-mediated ffERGs were undetectable, rod ERGs were ~80% of normal mean. Static perimetry showed severe central cone and rod dysfunction. Foveal to parafoveal hypoautofluorescence, most obvious on NIR-FAF, co-localized with outer segment shortening/loss and outer nuclear layer thinning by SD-OCT, and with reduced photoreceptors densities by AOSLO. A structural-functional dissociation was confirmed for cone- and rod-mediated parameters. Worsening of the above abnormalities was documented by SD-OCT and FAF in P2 at 3 years. Gene screening identified compound heterozygous mutations in BBS7 (p.Val266Glu: c.797 T > A of maternal origin; c.1781_1783delCAT, paternal) in both patients. Conclusions : BBS7 -associated retinal degeneration may present as a progressive cone-rod dystrophy pattern, reminiscent of both the murine and non-human primate models of the disease. Predominantly central retinal abnormalities in both cone and rod photoreceptors showed a structural-functional dissociation, an ideal scenario for gene augmentation treatments.

Details

Language :
English
ISSN :
1744-5094
Volume :
42
Issue :
3
Database :
MEDLINE
Journal :
Ophthalmic genetics
Publication Type :
Academic Journal
Accession number :
33729075
Full Text :
https://doi.org/10.1080/13816810.2021.1888132