Fig. 1From: A novel homozygous splice site variant in ARL2BP causes a syndromic autosomal recessive rod-cone dystrophy with situs inversus, asthenozoospermia, unilateral renal agenesis and microcystsVisual field extension with V/4e target in LE. Legend The patient has a stable fixation but approximately 5 degrees off-center to the bottom right. The residual visual field is slightly shifted to the temporal side. The test is reliableBack to article page