Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4133
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dc.contributor.authorFrancis, A.en
dc.contributor.authorBurke, J.en
dc.contributor.authorFrancis, L.en
dc.contributor.authorMcTaggart, S.en
dc.contributor.authorMallett, A.en
dc.date.accessioned2022-11-07T23:49:41Z-
dc.date.available2022-11-07T23:49:41Z-
dc.date.issued2016en
dc.identifier.citation9 , 2016, p. 88-93en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/4133-
dc.description.abstractBackground: Steroid resistant nephrotic syndrome (SRNS) is increasingly recognised to have a genetic basis following the identification of a number of mutations within genes encoding podocyte and basement membrane proteins. The ARHGAP24 gene product is a recently recognised important player in podocyte interaction with the glomerular basement membrane. The ARHGAP24 gene encodes a protein involved in regulating cell motility, membrane structure and polarity. Mutations in the gene have been showin vitro to cause cell membrane ruffling. Case Presentation: We report a novel missense mutation in exon 4 (c.[284G>A]; p.[Arg95Gln]) of the ARHGAP24 gene in a child that presented with SRNS at four years of age. Renal biopsy demonstrated unusual polypoid changes of the glomerular basement membrane (GBM). Conclusion: We propose this novel ARHGAP24 mutation as causative for SRNS associated with unusual polypoid basement membrane changes. These biopsy findings, in association with ARHGAP24 mutation and clinical nephrotic syndrome are a novel finding. This finding may advance the understanding of ARHGAP24 gene product function.L6127948352016-10-27 <br />2016-11-02 <br />en
dc.language.isoenen
dc.relation.ispartofOpen Urology and Nephrology Journalen
dc.titlePolypoid change of the glomerular basement membrane in a child with steroid resistant nephrotic syndrome and ARHGAP24 mutation: A case reporten
dc.typeArticleen
dc.identifier.doi10.2174/1874303X01609010088en
dc.subject.keywordshuman tissueen
dc.subject.keywordshyperactivityen
dc.subject.keywordsimmunofluorescenceen
dc.subject.keywordskidney biopsyen
dc.subject.keywordsmaleen
dc.subject.keywordsmembrane structureen
dc.subject.keywordsmembranous glomerulonephritisen
dc.subject.keywordsmissense mutationen
dc.subject.keywordshigh throughput sequencingen
dc.subject.keywordspreschool childen
dc.subject.keywordsRho gtpase activating protein 24 geneen
dc.subject.keywordssleep disorderen
dc.subject.keywordstachypneaen
dc.subject.keywordsbody weight gainen
dc.subject.keywordspriority journalen
dc.subject.keywordscreatininecyclophosphamideen
dc.subject.keywordsprednisoneen
dc.subject.keywordsRho factoren
dc.subject.keywordsRho gtpase activating protein 24en
dc.subject.keywordsserum albuminen
dc.subject.keywordsunclassified drugen
dc.subject.keywordsarticleen
dc.subject.keywordscase reporten
dc.subject.keywordscell motilityen
dc.subject.keywordschilden
dc.subject.keywordscongenital nephrotic syndromeen
dc.subject.keywordsfoot edemaen
dc.subject.keywordsgeneen
dc.subject.keywordsgenetic identificationen
dc.subject.keywordsglomerulus basement membraneen
dc.subject.keywordsglucose intoleranceen
dc.subject.keywordshumanen
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L612794835&from=exporthttp://dx.doi.org/10.2174/1874303X01609010088 |en
dc.identifier.risid1030en
dc.description.pages88-93en
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
Appears in Sites:Children's Health Queensland Publications
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