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. 2021 Feb 27;13:2515841421997191. doi: 10.1177/2515841421997191

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© The Author(s), 2021

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 1. — Representative illustrations of Bestrophinopathy fundus appearance. (a) Best disease, with the egg yolk-like vitelliform lesion observed at the macula. (b) Autosomal recessive bestrophinopathy, characterised by multifocal deposits and lesions around and beyond the macula. (c) Autosomal dominant vitreoretinochoroidopathy typified by presence of a hyperpigmented circumferential band of pigmentation in the peripheral retina. (d) Best-related retinitis pigmentosa characterised by the presence of peripheral pigment changes, bone spicules and foveal deposits.