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. Author manuscript; available in PMC: 2018 Feb 15.
Published in final edited form as: Med Res Arch. 2017 Sep 18;5(9):10.18103/mra.v5i9.1526.

Figure 1.

Figure 1

Right (20/100 best corrected visual acuity (BCVA)) and left (20/80 BCVA) fundus photographs of a 47-year-old male with BBS caused by a homozygous M390R mutation in BBS1 showing the characteristic macular atrophy and peripheral bone spicule pigmentation. This patient has a history of postaxial polydactyly of the lower extremities and first noted visual symptoms at age 14.