| Literature DB >> 28511423 |
Mahendra K Singh1, Sidharth Pradhan2, Priyanko Chakraborty2.
Abstract
Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive disorder characterized primarily by rod-cone dystrophy, postaxial polydactyly, central obesity, mental retardation, hypogonadism, and renal dysfunction. We present two cases of this syndrome, both female, who presented with complaints of nyctalopia and mental retardation, and additionally one of them had sensorineural hearing loss while the other had serous otitis media. Hearing loss being a rare presentation is worth reporting. Both the patients were given a course of vitamin A and the parents were counseled regarding the prognosis and additional complications associated with the syndrome.Entities:
Keywords: Hearing loss; Postaxial polydactyly; Rod-cone dystrophy; Serous otitis media
Year: 2017 PMID: 28511423 PMCID: PMC5427349 DOI: 10.7860/JCDR/2017/24499.9466
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X