Please use this identifier to cite or link to this item:
https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4133
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Francis, A. | en |
dc.contributor.author | Burke, J. | en |
dc.contributor.author | Francis, L. | en |
dc.contributor.author | McTaggart, S. | en |
dc.contributor.author | Mallett, A. | en |
dc.date.accessioned | 2022-11-07T23:49:41Z | - |
dc.date.available | 2022-11-07T23:49:41Z | - |
dc.date.issued | 2016 | en |
dc.identifier.citation | 9 , 2016, p. 88-93 | en |
dc.identifier.other | RIS | en |
dc.identifier.uri | http://dora.health.qld.gov.au/qldresearchjspui/handle/1/4133 | - |
dc.description.abstract | Background: 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.iso | en | en |
dc.relation.ispartof | Open Urology and Nephrology Journal | en |
dc.title | Polypoid change of the glomerular basement membrane in a child with steroid resistant nephrotic syndrome and ARHGAP24 mutation: A case report | en |
dc.type | Article | en |
dc.identifier.doi | 10.2174/1874303X01609010088 | en |
dc.subject.keywords | human tissue | en |
dc.subject.keywords | hyperactivity | en |
dc.subject.keywords | immunofluorescence | en |
dc.subject.keywords | kidney biopsy | en |
dc.subject.keywords | male | en |
dc.subject.keywords | membrane structure | en |
dc.subject.keywords | membranous glomerulonephritis | en |
dc.subject.keywords | missense mutation | en |
dc.subject.keywords | high throughput sequencing | en |
dc.subject.keywords | preschool child | en |
dc.subject.keywords | Rho gtpase activating protein 24 gene | en |
dc.subject.keywords | sleep disorder | en |
dc.subject.keywords | tachypnea | en |
dc.subject.keywords | body weight gain | en |
dc.subject.keywords | priority journal | en |
dc.subject.keywords | creatininecyclophosphamide | en |
dc.subject.keywords | prednisone | en |
dc.subject.keywords | Rho factor | en |
dc.subject.keywords | Rho gtpase activating protein 24 | en |
dc.subject.keywords | serum albumin | en |
dc.subject.keywords | unclassified drug | en |
dc.subject.keywords | article | en |
dc.subject.keywords | case report | en |
dc.subject.keywords | cell motility | en |
dc.subject.keywords | child | en |
dc.subject.keywords | congenital nephrotic syndrome | en |
dc.subject.keywords | foot edema | en |
dc.subject.keywords | gene | en |
dc.subject.keywords | genetic identification | en |
dc.subject.keywords | glomerulus basement membrane | en |
dc.subject.keywords | glucose intolerance | en |
dc.subject.keywords | human | en |
dc.relation.url | https://www.embase.com/search/results?subaction=viewrecord&id=L612794835&from=exporthttp://dx.doi.org/10.2174/1874303X01609010088 | | en |
dc.identifier.risid | 1030 | en |
dc.description.pages | 88-93 | en |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
Appears in Sites: | Children's Health Queensland Publications |
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