Akçay, Betül Ilkay SezginGüney, EsraÜnlü, CihanGencer, BaranÖzgürhan, Engin Bilge2025-01-272025-01-2720131307-1173https://hdl.handle.net/20.500.12428/14168Bardet Biedl syndrome is a rare autosomal recessive condition with a wide spectrum of clinical features. Major criterias for diagnosis, include retinal dystrophy, obesity, dystrophic extremities, hypogonadism, mental retardation and renal dysfunction. In this study, we aimed to present the clinical manifestations of retinal dystrophy due to Bardet Biedl syndrome in 9 years old and 17 years old siblings.eninfo:eu-repo/semantics/closedAccessBardet Biedl syndrome; Retinal dystrophyArticle721241262-s2.0-84885024948N/A