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

<div>Fundal photographs and chromatogram of a patient with severe phenotype of retinitis pigmentosa and harboring PRPF3 mutations (patient IV:12). Fundal photographs of the right eye (a, b) and the left eye (c, d), and chromatogram of the PRPF3 mutation (c.1481C&gt;T, p.T494M) is shown (e).</div>

Journal of Ophthalmology

fig4

Figure 4

Figure 4: PRPF3-Associated Autosomal Dominant Retinitis Pigmentosa and CYP4V2-Associated Bietti’s Crystalline Corneoretinal Dystrophy Coexist in a Multigenerational Chinese Family

Figure 4 | PRPF3-Associated Autosomal Dominant Retinitis Pigmentosa and CYP4V2-Associated Bietti’s Crystalline Corneoretinal Dystrophy Coexist in a Multigenerational Chinese Family 