Figure 3 | European Journal of Human Genetics

Figure 3

From: A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants

Figure 3

Fundus autofluorescence (FAF) imaging and foveal OCT scans of three patients with USH2A retinopathy. Three patterns were observed: (i) a hyperautofluorescent ring on FAF and preserved photoreceptor inner segment ellipsoid line in the area within the hyperautofluorescent ring on OCT (subject D8a; top row); (ii) central hyperautofluorescence on FAF and absent photoreceptor inner segment ellipsoid line on OCT (subject D17; middle row), and (iii) severely decreased autofluorescence on FAF and absent outer retina layers with thinning of the retinal pigment epithelium/Bruch’s membrane complex band (subject D19; bottom row). Y.o., years old.

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