Publication:
Branchio-Oto-Renal (BOR) Syndrome-an uncommon form of congenital deafness

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creativeworkseries.issnISSN (Print) : 1993-2979 | ISSN (Online) : 1993-2987
dc.contributor.authorKoirala, K
dc.contributor.authorGuragain, RPS
dc.contributor.authorBhusal, CL
dc.date.accessioned2026-06-29T05:57:44Z
dc.date.available2026-06-29T05:57:44Z
dc.date.issued2007
dc.descriptionK. Koirala Department of ENT and Head and Neck Surgery, T.U. Teaching Hospital, Maharajgunj, Kathmandu, Nepal R.P.S Guragain Department of ENT and Head and Neck Surgery, T.U. Teaching Hospital, Maharajgunj, Kathmandu, Nepal C.L Bhusal Department of ENT and Head and Neck Surgery, T.U. Teaching Hospital, Maharajgunj, Kathmandu, Nepal
dc.description.abstractAbstract Case report: Children with congenital deafness are common referrals to the Pediatric Otolaryngology unit of the Teaching Hospital. Branchio-Oto-Renal (BOR) Syndrome, an autosomal dominant syndromic form of deafness presents variably with the presence of auricular or preauricular pits in association with hearing loss, branchial sinuses and renal abnormalities ranging from renal hypoplasia to agenesis. Renal manifestations are least common and mostly missed. The present case report highlights a case of Branchio-Oto-Renal syndrome detected at the age of 5 years with unilateral renal agenesis and normal renal function. Keywords: Branchio-Oto-Renal syndrome, hearing loss, renal agenesis
dc.identifierhttps://doi.org/10.59779/jiomnepal.281
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6798
dc.language.isoen_US
dc.publisherInstitute of Medicine
dc.subjectBranchio-Oto-Renal syndrome
dc.subjecthearing loss
dc.subjectrenal agenesis
dc.titleBranchio-Oto-Renal (BOR) Syndrome-an uncommon form of congenital deafness
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage50
oaire.citation.startPage48
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