PRPF3-Associated Autosomal Dominant Retinitis Pigmentosa and CYP4V2-Associated Bietti’s Crystalline Corneoretinal Dystrophy Coexist in a Multigenerational Chinese Family

Figure 3

Fundal images and chromatograms of the proband with a clinical diagnosis with Bietti’s crystalline corneoretinal dystrophy and harboring compound heterozygous mutations in the CYP4V2 gene (patient VI:1). Fundal photographs (a, b), autofluorescence images (c, d), and near-infrared images (e, f) of both eyes are shown on the left, and chromatograms of two mutations are demonstrated on the right (g, h).

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