Vascular and structural analyses of retinal and choroidal alterations in Fabry disease: the effect of hyperreflective foci and retinal vascular tortuosity
Author:
Affiliation:
1. Department of Ophthalmology, Ankara University School of Medicine, Ankara, Turkey
2. Department of Pediatric Metabolism and Nutrition, Hacettepe University Faculty of Medicine, Ankara, Turkey
Funder
financial support
Publisher
Informa UK Limited
Subject
Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/13816810.2022.2025607
Reference35 articles.
1. Fabry Disease Practice Guidelines: Recommendations of the National Society of Genetic Counselors
2. Female Fabry disease patients and X-chromosome inactivation
3. X-chromosome inactivation in female patients with Fabry disease
4. Ocular Signs Correlate Well with Disease Severity and Genotype in Fabry Disease
5. Fabry disease in children: correlation between ocular manifestations, genotype and systemic clinical severity
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1. Ocular Manifestations of Fabry Disease: Report from a Tertiary Eye Care Center in Türkiye;Turkish Journal of Ophthalmology;2024-06-28
2. Retinal Vascular Tortuosity Index Change after Idiopathic Epiretinal Membrane Surgery: Does Internal Limiting Membrane Peeling Affect Retinal Vascular Tortuosity?;Diagnostics;2023-02-20
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