Fig. 1
From: Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss
Pedigrees and audiological data of families that were recruited through either a hereditary hearing loss or eye study, or the medical genetics clinic. a) Family R2100 is a hereditary hearing loss pedigree with multiple affected sibships. Usher syndrome type 2C was not apparent at ascertainment, b) Serial audiograms of PID V-2 and V3 (Family R2100), c) Family R4110 was recruited to this study by our local medical genetics clinic. The proband of this family did not pass newborn hearing screens and was GJB2-negative, d) Audioprofiles of Usher syndrome type 2A families, e) Family R0723 is an Usher syndrome pedigree with several affected members