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

Figure 1

Pedigree plot. The proband is indicated by an arrow. One affected patient with red solid box showed clinical findings compatible to the diagnosis of Bietti’s crystalline corneoretinal dystrophy (VI:1), and the other affected members with black solid box presented clinical features of retinitis pigmentosa. Males and females are represented by squares and circles, respectively. Filled symbols: affected members; open symbols: unaffected members.