Clinical Study

Multimodal Imaging in Hereditary Retinal Diseases

Figure 5

Fundus photograph of an autosomal recessive bestrophinopathy shows a well-demarcated area with round yellowish-white deposits at the posterior pole and along the superotemporal arcade; subretinal fibrosis is visible inferior nasal of the fovea. SD-OCT scan illustrates extensive RPE deposits extending to the outer plexiform layer. Fundus autofluorescence imaging displayed marked hyperautofluorescence corresponding to the yellow lesions. Fundus photograph shows a well-demarcated area with round yellowish-white deposits at the posterior pole extending to the superior periphery. SD-OCT scan demonstrates RPE detachment from the photoreceptors. Photoreceptor outer segments are thickened and elongated. Fundus autofluorescence identified additional peripapillary hyperfluorescent deposits not seen on funduscopy.
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