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Clinical images from patients with mutations in the PRPH2 and ABCA4 genes. (A) Fundus and (B) autofluorescence of a case from F2-III-6 (PRPH2: p.Arg46Ter and ABCA4: p.Leu2027Phe and p.Gly1977Ser) with the typical appearance of ECA and foveal preservation that explains the good visual acuity. (C) The ocular fundus and (D) AF of an F3-V-2 member (PRPH2: p.Lys154del and ABCA4: p.Arg2030Gln), which resembles FF.
