dc.contributor.author | Rajoor, Umesh G. | |
dc.contributor.author | Gundikeri, Shiddappa | |
dc.contributor.author | Sindhur, Jayaraj C. | |
dc.contributor.author | Dhananjaya, M. | |
dc.date.accessioned | 2015-07-26T19:42:19Z | |
dc.date.available | 2015-07-26T19:42:19Z | |
dc.date.issued | 2013-12 | |
dc.identifier.citation | Medica Innovatica. 2013 Dec; 2(2): 118-120. | en_US |
dc.identifier.issn | 2278-7526, 2320-7582 | |
dc.identifier.uri | http://hdl.handle.net/123456789/645 | |
dc.description.abstract | Bardet Biedl syndrome (BBS) is a rare autosomal recessive condition characterised by rod-cone dystrophy, postaxial polydactyly, central obesity, mental retardation, learning difficulties, hypogonadism in males and renal involvement. Renal failure is the most common cause for morbidity and mortality in such individuals. We report the case of BBS with chronic renal failure from north Karnataka. | en_US |
dc.language.iso | en | en_US |
dc.publisher | B.V.V. Sangha’s S. Nijalingappa Medical College | en_US |
dc.subject | Bardet-Biedl syndrome | en_US |
dc.subject | Autosomal recessive | en_US |
dc.subject | Renal failure | en_US |
dc.title | Bardet biedl syndrome-a rare case report from North Karnataka | en_US |
dc.type | Article | en_US |