Ophthalmoscopy of the right and left eye of Case 1, showing a normal macula with a slight reduction of the foveal reflex (a, c). SD-OCT showed a maintained foveal contour, juxtafoveal microcystic cavities in the outer retina, increased foveal rod-shaped full-thickness hyperreflectivity that extended from the outer segments of the photoreceptors and RPE to the inner layer of the retina, and a slight interruption of the external limiting membrane and of the inner and outer segment (IS/OS) junctions, with disorganized material in the “vitelliform space” (b, d).