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Article: Glomerulonephropathy of Laurence-Moon-Biedl syndrome

TitleGlomerulonephropathy of Laurence-Moon-Biedl syndrome
Authors
Cheng, IKPChan, KWChan, MKKung, AMa, JWang, C
Issue Date1988
PublisherB M J Publishing Group. The Journal's web site is located at http://www.postgradmedj.com
Citation
Postgraduate Medical Journal, 1988, v. 64 n. 754, p. 621-625 How to Cite?
DOI: http://dx.doi.org/10.1136/pgmj.64.754.621
AbstractA patient with Laurence-Moon-Biedl syndrome and nephrotic range proteinuria is presented. Radiological investigation of the urinary tract revealed clubbed calyces but no evidence of obstruction or vesicoureteric reflux. Renal biopsy revealed occasional sclerotic glomeruli, extensive foot-process fusion and segmental glomerular basement membrane abnormalities with negative immunofluorescence for immunoglobulins and complement. Nephrotic proteinuria responded to steroid therapy but mild proteinuria persisted. The findings were consistent with minimal change nephropathy superimposed on the glomerular lesions of Lawrence-Moon-Biedl syndrome.
Persistent Identifierhttp://hdl.handle.net/10722/44991
ISSN
0032-5473
2023 Impact Factor: 3.6
2023 SCImago Journal Rankings: 0.876
PubMed Central ID
PMC2428942
ISI Accession Number ID
WOS:A1988P754400014

 

DC FieldValueLanguage
dc.contributor.authorCheng, IKPen_HK
dc.contributor.authorChan, KWen_HK
dc.contributor.authorChan, MKen_HK
dc.contributor.authorKung, Aen_HK
dc.contributor.authorMa, Jen_HK
dc.contributor.authorWang, Cen_HK
dc.date.accessioned2007-10-30T06:15:09Z-
dc.date.available2007-10-30T06:15:09Z-
dc.date.issued1988en_HK
dc.identifier.citationPostgraduate Medical Journal, 1988, v. 64 n. 754, p. 621-625en_HK
dc.identifier.issn0032-5473en_HK
dc.identifier.urihttp://hdl.handle.net/10722/44991-
dc.description.abstractA patient with Laurence-Moon-Biedl syndrome and nephrotic range proteinuria is presented. Radiological investigation of the urinary tract revealed clubbed calyces but no evidence of obstruction or vesicoureteric reflux. Renal biopsy revealed occasional sclerotic glomeruli, extensive foot-process fusion and segmental glomerular basement membrane abnormalities with negative immunofluorescence for immunoglobulins and complement. Nephrotic proteinuria responded to steroid therapy but mild proteinuria persisted. The findings were consistent with minimal change nephropathy superimposed on the glomerular lesions of Lawrence-Moon-Biedl syndrome.en_HK
dc.format.extent990956 bytes-
dc.format.extent2438 bytes-
dc.format.extent1955 bytes-
dc.format.mimetypeapplication/pdf-
dc.format.mimetypetext/plain-
dc.format.mimetypetext/plain-
dc.languageengen_HK
dc.publisherB M J Publishing Group. The Journal's web site is located at http://www.postgradmedj.comen_HK
dc.relation.ispartofPostgraduate Medical Journalen_HK
dc.rightsPostgraduate Medical Journal. Copyright © B M J Publishing Group.en_HK
dc.subject.meshKidney-ultrastructureen_HK
dc.subject.meshLaurence-Moon-Syndrome-pathologyen_HK
dc.subject.meshNephrosis,-Lipoid-pathologyen_HK
dc.titleGlomerulonephropathy of Laurence-Moon-Biedl syndromeen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0032-5473&volume=64&issue=754&spage=621&epage=625&date=1988&atitle=Glomerulonephropathy+of+Laurence-Moon-Biedl+syndromeen_HK
dc.identifier.emailChan, KW:hrmtckw@hku.hken_HK
dc.identifier.emailKung, A:awckung@hku.hken_HK
dc.identifier.authorityChan, KW=rp00330en_HK
dc.identifier.authorityKung, A=rp00368en_HK
dc.description.naturepublished_or_final_versionen_HK
dc.identifier.doi10.1136/pgmj.64.754.621-
dc.identifier.pmid3249710en_HK
dc.identifier.pmcidPMC2428942-
dc.identifier.scopuseid_2-s2.0-0023809388en_HK
dc.identifier.volume64en_HK
dc.identifier.issue754en_HK
dc.identifier.spage621en_HK
dc.identifier.epage625en_HK
dc.identifier.isiWOS:A1988P754400014-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridCheng, IKP=7102537483en_HK
dc.identifier.scopusauthoridChan, KW=16444133100en_HK
dc.identifier.scopusauthoridChan, MK=7402597821en_HK
dc.identifier.scopusauthoridKung, A=7102322339en_HK
dc.identifier.scopusauthoridMa, J=24491943700en_HK
dc.identifier.scopusauthoridWang, C=8266261300en_HK
dc.identifier.issnl0032-5473-

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