Publication:
Differentiating Gilbert Syndrome from Crigler Najjar Syndrome Type 2 by Phenobarbitone Test

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorSinha, R
dc.contributor.authorDalal, S
dc.contributor.authorSodhi, K
dc.date.accessioned2026-03-23T09:50:27Z
dc.date.available2026-03-23T09:50:27Z
dc.date.issued2015
dc.descriptionR Sinha Department of Pediatrics, Military Hospital Jodhpu S Dalal Department of Paediatrics, AFMC Pune K Sodhi Department of Paediatrics, Command Hospital, Chandigarh
dc.description.abstractAbstract: Gilbert syndrome characterized by jaundice with intermittent elevations of indirect bilirubin, in the absence of haemolysis or underlying liver disease, has both autosomal dominant and recessive inheritance. Crigler-Najjar syndrome type II (CNS2) is a hereditary disorder of bilirubin metabolism characterized by unconjugated hyperbilirubinemia due to reduced and inducible activity of hepatic bilirubin glucuronosyltransferase (GT). We report 20 children between age 5 to 15 years with unconjugated hyperbilirubenemia who were given seven days of oral phenobarbitone (5mg/kg/day) and decrease in level of bilirubin was noted. There was only 30-40% reduction of bilirubin in Crigler Najjar Syndrome Type 2 compared to Gilberts Syndrome in which bilirubin level normalised. This case series highlights the importance of simple test to differentiate these two conditions. This test is also very helpful in a place where enzyme level and mutational study cannot be done.
dc.identifierhttps://doi.org/10.3126/jnps.v35i1.10620
dc.identifier.urihttps://hdl.handle.net/20.500.14572/5360
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectGilberts
dc.subjectCrigler Najjar
dc.subjecthyperbilirubinemia
dc.titleDifferentiating Gilbert Syndrome from Crigler Najjar Syndrome Type 2 by Phenobarbitone Test
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage84
oaire.citation.startPage82
relation.isJournalIssueOfPublication5a1d626f-003d-4bd6-a558-b7a82329ac4e
relation.isJournalIssueOfPublication.latestForDiscovery5a1d626f-003d-4bd6-a558-b7a82329ac4e
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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