After reevaluation, the clinical diagnosis for patient 2016090902 who carried the novel compound heterozygous mutations NM_024685.3:c.1063C>T:p.(Gln355Ter) and NM_024685.3: c.378G>A:p.(Trp126Ter) in BBS10, was revised to Bardet–Biedl syndrome. The gene discussed is BBS10; the disease is Bardet-Biedl syndrome.