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Fig. 2 | Renal Replacement Therapy

Fig. 2

From: Genetic analysis diagnosed Bardet–Biedl syndrome in a patient with a clinical diagnosis of Senior–Løken syndrome

Fig. 2

Disease 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, nephronophthisis

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