GILBERT SYNDROME: GENETIC FACTORS AND DIAGNOSTIC APPROACHES

dc.contributor.author	Malika Khusаnovna Tаlibdjаnova
dc.date.accessioned	2025-12-29T18:00:00Z
dc.date.issued	2025-09-30
dc.description.abstract	Gilbert syndrome (GS) is an inherited disorder of bilirubin metabolism characterized by unconjugated hyperbilirubinemia. The condition is associated with a mutation in the promoter region of the UGT1A1 gene, which encodes the enzyme uridine diphosphate-glucuronosyltransferase 1A1. Although often asymptomatic, accurate diagnosis of GS is important to prevent misdiagnosis, unnecessary investigations, and overtreatment.
dc.format	application/pdf
dc.identifier.uri	https://webofjournals.com/index.php/5/article/view/5138
dc.identifier.uri	https://asianeducationindex.com/handle/123456789/24877
dc.language.iso	eng
dc.publisher	Web of Journals Publishing
dc.relation	https://webofjournals.com/index.php/5/article/view/5138/5173
dc.rights	https://creativecommons.org/licenses/by-nc-nd/4.0
dc.source	Web of Medicine: Journal of Medicine, Practice and Nursing ; Vol. 3 No. 9 (2025): WOM; 189-190
dc.source	2938-3765
dc.title	GILBERT SYNDROME: GENETIC FACTORS AND DIAGNOSTIC APPROACHES
dc.type	info:eu-repo/semantics/article
dc.type	info:eu-repo/semantics/publishedVersion
dc.type	Peer-reviewed Article

item.page.files

pagination.showing.labelpagination.showing.detail

item.page.filesection.name: tlibdjnova_2025_gilbert_syndrome_genetic_factors_and_dia.pdf
item.page.filesection.size: 286.6 KB
item.page.filesection.format: Adobe Portable Document Format