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). The gene discussed is CFAP410; the disease is Rod-cone dystrophy.