Fig. 2
From: Novel mutations of the USH2A gene cause Usher syndrome in five Chinese families
Clinical phenotype of F3-II-2. UW-FP demonstrated midperipheral pigment migration and attenuated retinal vessels (a). FAF demonstrated midperipheral and macular patchy hypoautofluorescence (b). The macular GCC was thinned, while the RNFL was normal in both eyes (c). Macular OCTA demonstrated a decreasing vascular flow density (superficial and deep). The FAZ of both the superficial plexus and deep capillary plexus was enlarged, and central foveal thinning and loss of photoreceptors were evident (d)