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Retinal Dysfunction in Carriers of Bardet-Biedl Syndrome
- Source :
- Ophthalmic Genetics. 28:163-168
- Publication Year :
- 2007
- Publisher :
- Informa UK Limited, 2007.
-
Abstract
- To determine whether retinal dysfunction in obligate carriers of the Bardet-Biedl syndrome (BBS) could be observed in local electroretinographic responses obtained with the multifocal electroretinogram (mfERG).Six obligate carriers of the BBS were examined for the study. Examination of each carrier included an ocular examination and mfERG testing of one eye. For the mfERG, we used a 103-scaled hexagonal stimulus array that subtended a retinal area of approximately 40 degrees in diameter. The amplitudes and implicit times in each location for the mfERG were compared with the corresponding values determined for a group of 34 normally sighted, age-similar control subjects.Mapping of 103 local electroretinographic response amplitudes within a central 40 degrees area with the mfERG showed regions of reduced mfERG amplitudes in three of six carriers. Implicit time measurements in the 6 carriers were all normal except for those locations associated with abnormal amplitude reductions in 3 of the carriers. When present, retinal dysfunction was evident in the presence of a normal-appearing fundus.Multifocal ERG testing can demonstrate areas of retinal dysfunction in carriers of the BBS. This test may therefore be useful for identifying some heterozygous carriers of this disease.
- Subjects :
- Adult
Heterozygote
medicine.medical_specialty
Visual acuity
genetic structures
Visual Acuity
Audiology
Biology
Retina
chemistry.chemical_compound
Bardet–Biedl syndrome
Electroretinography
medicine
Humans
Bardet-Biedl Syndrome
Genetics (clinical)
medicine.diagnostic_test
Hexagonal crystal system
Retinal
Middle Aged
Control subjects
medicine.disease
eye diseases
Ophthalmology
Retinal dysfunction
medicine.anatomical_structure
chemistry
Pediatrics, Perinatology and Child Health
sense organs
medicine.symptom
Subjects
Details
- ISSN :
- 17445094 and 13816810
- Volume :
- 28
- Database :
- OpenAIRE
- Journal :
- Ophthalmic Genetics
- Accession number :
- edsair.doi.dedup.....426ce297bfdd35fc7bca58b544af6120
- Full Text :
- https://doi.org/10.1080/13816810701537440