Previously, pathogenic CFAP410 variants have been described with retinitis pigmentosa or cone rod dystrophy phenotypes, mostly in association with systemic skeletal abnormalities such as reduced stature, small and narrow thoraces, pelvic bone malformations, hip dysplasia, scoliosis, and platyspondyly (4,5,8,9). This evidence concerns the gene CFAP410 and cone-rod dystrophy.