Achromatopsia: case presentation and literature review emphasising the value of spectral domain optical coherence tomography
Author:
Affiliation:
1. Nova Southeastern University, Fort Lauderdale, Florida, USA,
Publisher
Informa UK Limited
Subject
Optometry,Ophthalmology
Link
https://www.tandfonline.com/doi/pdf/10.1111/cxo.12175
Reference15 articles.
1. Progressive Cone and Cone-Rod Dystrophies: Phenotypes and Underlying Molecular Genetic Basis
2. CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders
3. A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia
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1. Quantitative and qualitative characterization of retinal dystrophies in canine models of inherited retinal diseases using spectral domain optical coherence tomography (SD-OCT);Experimental Eye Research;2022-07
2. A new mutation in the PDE6C gene in achromatopsia;European Journal of Ophthalmology;2022-04-14
3. Measurement of macular thickness with optical coherence tomography: impact of using a paediatric reference database and analysis of interocular symmetry;Graefe's Archive for Clinical and Experimental Ophthalmology;2020-08-29
4. Central serous chorioretinopathy and achromatopsia: a case report;Documenta Ophthalmologica;2020-05-18
5. The use of contact lenses in low vision rehabilitation: optical and therapeutic applications;Clinical and Experimental Optometry;2017-09-01
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