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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.
- Source :
-
Ophthalmic genetics [Ophthalmic Genet] 2021 Jun; Vol. 42 (3), pp. 252-265. Date of Electronic Publication: 2021 Mar 17. - Publication Year :
- 2021
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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.
- Subjects :
- Adult
Bardet-Biedl Syndrome diagnostic imaging
Bardet-Biedl Syndrome physiopathology
Cone-Rod Dystrophies diagnostic imaging
Cone-Rod Dystrophies physiopathology
Electroretinography
Genetic Therapy
Humans
Male
Models, Animal
Mutation genetics
Ophthalmoscopy
Optical Imaging
Phenotype
Retina physiopathology
Siblings
Tomography, Optical Coherence
Visual Acuity
Visual Field Tests
Young Adult
Adaptor Proteins, Signal Transducing genetics
Bardet-Biedl Syndrome genetics
Cone-Rod Dystrophies genetics
Cytoskeletal Proteins genetics
Subjects
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