Publication:
Siblings with Bardet Beidl Syndrome

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorPeter, Ram
dc.contributor.authorPeter, Ram
dc.contributor.authorJose, Priya
dc.contributor.authorNair, MNG
dc.date.accessioned2026-05-22T10:53:05Z
dc.date.available2026-05-22T10:53:05Z
dc.date.issued2013
dc.descriptionRam 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, Pondicherry
dc.description.abstractAbstract: 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.
dc.identifierhttps://doi.org/10.3126/jnps.v33i3.8081
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6222
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectBardet Beidl Syndrome
dc.subjecthypothyroidism
dc.subjectretinal degeneration
dc.titleSiblings with Bardet Beidl Syndrome
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage238
oaire.citation.startPage236
relation.isJournalIssueOfPublication8144a486-a616-4200-bdbc-b5f191c661df
relation.isJournalIssueOfPublication.latestForDiscovery8144a486-a616-4200-bdbc-b5f191c661df
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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