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. 2023 Jul 11;10:33. doi: 10.1186/s40662-023-00349-y

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 6 — Clinical characteristics of central serous chorioretinopathy detected by optical coherence tomography angiography (OCTA). Automated segmentation of the superficial retina (at a range of 3 × 3 mm) showing foveal lesions on the topographic map. Focal protrusion of retinal pigment epithelium and high-density area of the choriocapillaris layer that corresponded to serous retinal detachment (black arrows) has also been noted (a, b). c Automated segmentation of the deep retina of the right eye. d Thickness map of automated segmentation of the deep retina of the right eye. The lesion which was showing by the white arrows in (c) and black arrows in (d) corresponded to serous retinal detachment which was indicated by black arrows in (b)