Optical coherence tomography findings in occult macular dystrophy
- PMID: 17317401
- DOI: 10.1016/j.ajo.2006.10.025
Optical coherence tomography findings in occult macular dystrophy
Abstract
Purpose: To determine the basis for unexplained visual acuity loss in selected patients.
Design: Observational study of patients with unexplained reduced visual acuity.
Methods: We used optical coherence tomography (OCT) to evaluate foveal structure in eight patients. These patients had corrected visual acuities of 20/25 to count fingers in one or both eyes and a normal ocular examination. We recorded foveal cone electroretinograms (ERGs) as an objective measure of foveal function.
Results: Seven patients showed reduced foveal thickness associated with thinning of the outer nuclear layer (ONL), and five of these patients also had reduced foveal cone ERGs. One patient had normal tomograms and reduced foveal ERGs.
Conclusions: Unexplained reductions in visual acuity may result from photoreceptor loss or foveal malfunction without photoreceptor loss, which are indicators of occult macular dystrophy. OCT and the foveal cone ERG together appear to be sufficient to identify the basis for visual acuity loss in these patients.
Similar articles
-
Morphologic photoreceptor abnormality in occult macular dystrophy on spectral-domain optical coherence tomography.Invest Ophthalmol Vis Sci. 2010 Jul;51(7):3673-9. doi: 10.1167/iovs.09-4169. Epub 2010 Feb 17. Invest Ophthalmol Vis Sci. 2010. PMID: 20164460
-
Foveal photoreceptor layer in eyes with persistent cystoid macular edema associated with branch retinal vein occlusion.Am J Ophthalmol. 2008 Feb;145(2):273-280. doi: 10.1016/j.ajo.2007.09.019. Epub 2007 Nov 28. Am J Ophthalmol. 2008. PMID: 18045566
-
Three-dimensional imaging of the foveal photoreceptor layer in central serous chorioretinopathy using high-speed optical coherence tomography.Ophthalmology. 2007 Dec;114(12):2197-207. doi: 10.1016/j.ophtha.2007.02.015. Epub 2007 May 15. Ophthalmology. 2007. PMID: 17507096
-
Occult macular dystrophy.Jpn J Ophthalmol. 2015 Mar;59(2):71-80. doi: 10.1007/s10384-015-0371-7. Epub 2015 Feb 10. Jpn J Ophthalmol. 2015. PMID: 25665791 Review.
-
Foveal photoreceptor disruption in ocular diseases: An optical coherence tomography-based differential diagnosis.Surv Ophthalmol. 2023 Jul-Aug;68(4):655-668. doi: 10.1016/j.survophthal.2023.03.003. Epub 2023 Mar 18. Surv Ophthalmol. 2023. PMID: 36934831 Review.
Cited by
-
Rare occult macular dystrophy with a pathogenic variant in the RP1L1 gene in a patient of Swiss descent.Am J Ophthalmol Case Rep. 2022 Apr 10;26:101527. doi: 10.1016/j.ajoc.2022.101527. eCollection 2022 Jun. Am J Ophthalmol Case Rep. 2022. PMID: 35464678 Free PMC article.
-
ERG and OCT findings of a patient with a clinical diagnosis of occult macular dystrophy in a patient of Ashkenazi Jewish descent associated with a novel mutation in the gene encoding RP1L1.BMJ Case Rep. 2017 May 4;2017:bcr2016218364. doi: 10.1136/bcr-2016-218364. BMJ Case Rep. 2017. PMID: 28473427 Free PMC article.
-
Structural and functional evaluation of macula in a 9-year-old boy with occult macular dystrophy and his affected elder sibling.Oman J Ophthalmol. 2016 Jan-Apr;9(1):55-8. doi: 10.4103/0974-620X.176103. Oman J Ophthalmol. 2016. PMID: 27013831 Free PMC article.
-
Pattern-reversal visual-evoked potential in patients with occult macular dystrophy.Clin Ophthalmol. 2010 Dec 10;4:1515-20. doi: 10.2147/OPTH.S15088. Clin Ophthalmol. 2010. PMID: 21191449 Free PMC article.
-
Characterizing the phenotype and genotype of a family with occult macular dystrophy.Arch Ophthalmol. 2012 Dec;130(12):1554-9. doi: 10.1001/archophthalmol.2012.2683. Arch Ophthalmol. 2012. PMID: 23229695 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical