Peter, RamPeter, RamJose, PriyaNair, MNG2026-05-222026-05-222013https://hdl.handle.net/20.500.14572/6222Ram Peter Resident, Department of Paediatrics, Pondicherry Institute of Medical Sciences, Pondicherry Priya Jose Department of Paediatrics, Pondicherry Institute of Medical Sciences, Pondicherry MNG Nair Professor and Head of Department, Department of Paediatrics, Pondicherry Institute of Medical Sciences, PondicherryAbstract: Bardet Biedl syndrome is an autosomal recessive condition affecting many parts of the body. Incidence of BBS is 1 in 100000. Its clinical features varies in person to person though from same family too. We are reporting two siblings with Bardet Beidl syndrome with different clinical presentation.en-USBardet Beidl Syndromehypothyroidismretinal degenerationArticle