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Klin Monbl Augenheilkd 2020; 237(04): 484-486
DOI: 10.1055/a-1068-2762
DOI: 10.1055/a-1068-2762
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Publication History
received 26 September 2019
accepted 27 October 2019
Publication Date:
24 February 2020 (online)


Background
Enhanced S-cone syndrome (ESCS) is an autosomal recessive retinal dystrophy associated with a NR2E3 mutation, causing night blindness, decreased visual acuity, and visual field defects [1]. Clinically, ESCS is characterized by annular pigmentation along the vascular arcades and macular abnormalities [2]. Best vitelliform macular dystrophy (BVMD) is also an autosomal but dominant hereditary retinal dystrophy associated with the BEST1 gene, which affects central vision with a relatively good prognosis and presents macular egg yolk yellow lesions [3].