Fig. 4From: A novel homozygous splice site variant in ARL2BP causes a syndromic autosomal recessive rod-cone dystrophy with situs inversus, asthenozoospermia, unilateral renal agenesis and microcystsRetinal dystrophy progression over time followed by BCVA and visual field extension. Legend Graph (A) shows the progressive decline of BCVA over 30 years of disease, from diagnosis (33 years old) to the last evaluation (63 years old). Graph (B) highlights the progressive loss of visual field, expressed as maximum radius extension in both eyes. The numerical data are reported in the corresponding tables on the right. * 2.30 LogMar corresponds to Hand Motion. **2.70 LogMar corresponds to Light PerceptionBack to article page