Fig. 2From: Genetic analysis diagnosed Bardet–Biedl syndrome in a patient with a clinical diagnosis of Senior–Løken syndromeDisease concepts of SLS, BBS, and NPHP-RC patients carrying SDCCAG8 mutations. Major symptoms of SLS, BBS, and NPHP-RC patients carrying SDCCAG8 mutations are described. No polydactyly has been reported among NPHP-RC patients with SDCCAG8 mutations. Asthma and otitis media are common symptoms of ciliopathy and are frequently reported in NPHP-RC patients with SDCCAG8 mutations. NPHP, nephronophthisisBack to article page