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Fig. 2 | BMC Ophthalmology

Fig. 2

From: Whole-exome sequencing reveals a novel CHM gene mutation in a family with choroideremia initially diagnosed as retinitis pigmentosa

Fig. 2

Images of fundus changes in the proband IV-2 and another affected male IV-5. Areas of retinal pigment epithelium (RPE) disrupted, chorioretinal atrophy, loss of choriocapillaris, and scattered bone-spicule pigment deposits partially covering the central macula in IV-2. Less severe chorioretinal atrophy and much less bone-spicule pigment deposits with preservation of the central macula in the younger patient IV-5

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