Correction: Correlation of retinal vascular characteristics with laboratory and ocular findings in Fabry disease: exploring ocular diagnostic biomarkers (Orphanet Journal of Rare Diseases, (2023), 18, 1, (314), 10.1186/s13023-023-02932-x)
Lindziute M, Kaufeld J, Hufendiek K, Volkmann I, Brockmann D, Hosari S, Hohberger B, Mardin C, Framme C, Tode J, Hufendiek K (2026)
Publication Type: Journal article, Erratum
Publication year: 2026
Journal
Book Volume: 21
Article Number: 188
Journal Issue: 1
DOI: 10.1186/s13023-025-04162-9
Abstract
https://doi.org/10.1186/s13023-023-02932-x. Following publication of the original article [1], the authors reported that the names and family names of the authors Christian Mardin and Jan Tode had been mistakenly reversed. The corrected names provided in this Correction is accurate. Additionally, the authors identified imprecise use of terminology regarding Lyso-Gb3 concentration and GLA enzyme activity. In several instances, these were incorrectly referred to as “LysoGb3 activity” and “GLA concentration”. This has also been corrected. The original article [1] has been updated.
Authors with CRIS profile
Sami Hosari
Department of Surgery
Bettina Hohberger
Department of Ophthalmology
Christian Mardin
Department of Ophthalmology
Involved external institutions
Germany (DE)How to cite
APA:
Lindziute, M., Kaufeld, J., Hufendiek, K., Volkmann, I., Brockmann, D., Hosari, S.,... Hufendiek, K. (2026). Correction: Correlation of retinal vascular characteristics with laboratory and ocular findings in Fabry disease: exploring ocular diagnostic biomarkers (Orphanet Journal of Rare Diseases, (2023), 18, 1, (314), 10.1186/s13023-023-02932-x). Orphanet Journal of Rare Diseases, 21(1). https://doi.org/10.1186/s13023-025-04162-9
MLA:
Lindziute, Migle, et al. "Correction: Correlation of retinal vascular characteristics with laboratory and ocular findings in Fabry disease: exploring ocular diagnostic biomarkers (Orphanet Journal of Rare Diseases, (2023), 18, 1, (314), 10.1186/s13023-023-02932-x)." Orphanet Journal of Rare Diseases 21.1 (2026).
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