Title:
Bardet biedl syndrome – A report of two cases with otolaryngologic symptoms

dc.contributor.authorMahendra K. Singh
dc.contributor.authorShrinkhal
dc.contributor.authorSidharth Pradhan
dc.contributor.authorPriyanko Chakraborty
dc.date.accessioned2026-02-07T08:31:34Z
dc.date.issued2017
dc.description.abstractBardet-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. © 2017, Journal of Clinical and Diagnostic Research. All rights reserved.
dc.identifier.doi10.7860/JCDR/2017/24499.9466
dc.identifier.issn2249782X
dc.identifier.urihttps://doi.org/10.7860/JCDR/2017/24499.9466
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/30940
dc.publisherJournal of Clinical and Diagnostic Research
dc.subjectHearing loss
dc.subjectPostaxial polydactyly
dc.subjectRod-cone dystrophy
dc.subjectSerous otitis media
dc.titleBardet biedl syndrome – A report of two cases with otolaryngologic symptoms
dc.typePublication
dspace.entity.typeArticle

Files

Collections