Figure 4 | European Journal of Human Genetics

Figure 4

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

Figure 4

Variability in the severity of ocular and audiological phenotype due to mutations in USH2A in three patients of similar age. Fundus autofluorescence (FAF) imaging and foveal OCT show a better preserved retina in subject D2 (group 3 corresponding to abnormal audiological assessment) and in a patient with Usher syndrome type II compared with subject D3 (middle panel), who has normal hearing.

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