Clinical Study

Multimodal Imaging in Hereditary Retinal Diseases

Figure 6

Color fundus photography of a patient with enhanced s-cone syndrome showing nummular pigmentary clumping at the level of the RPE along the vascular arcades and macular disturbance with subtle pigmentary changes; fundus autofluorescence shows an absence of AF outside the arcades and a ring of increased AF at the posterior pole. Foveal schisis is demonstrated on SD-OCT and confirmed by the absence of leakage on fluorescein angiography.
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