Insulin-like growth factor-1, growth hormone-dependent insulin-like growth factor-binding protein and growth in children with chronic renal failure
Identifieur interne : 000A29 ( Main/Corpus ); précédent : 000A28; suivant : 000A30Insulin-like growth factor-1, growth hormone-dependent insulin-like growth factor-binding protein and growth in children with chronic renal failure
Auteurs : M. Hodson ; Shane Brown ; Paul Roy ; R. RosenbergSource :
- Pediatric Nephrology [ 0931-041X ] ; 1992-09-01.
Abstract
Abstract: Insulin-like growth factor-binding protein-3 (IGFBP-3) and insulin-like growth factor-1 (IGF-1) levels were measured by specific radioimmunoassays in children with all degrees of chronic renal failure (CRF). Study group 1 comprised 29 children (10 on dialysis) who had been studied one to four times over 2 years to determine whether IGF-1 and IGFBP-3 levels differed from those in age-matched healthy children and to examine the relationship between these levels and heights. IGF-1 and IGFBP-3 levels did not differ from those in normal children. IGF-1 and IGFBP-3 were significantly correlated, increased with pubertal stage in all children and with age in non-dialysis patients. IGF-1, but not IGFBP-3, correlated with age in dialysis patients. There was no correlation between IGF-1 or IGFBP-3 levels (corrected for age) and height standard deviation score (SDS) in either non-dialysis or dialysis patients. Study group 2 comprised 19 children (7 on dialysis) who were studied prospectively for 1–2 years to examine the relationship between IGF-1 and IGFBP-3 levels, growth rates and nutritional parameters. Mean values of IGF-1 and IGFBP-3 (corrected for age) did not change over 1-year periods, while height SDS fell by −0.38 ±0.21 SD/year in dialysis patients and by −0.11 ±0.29 SD/year in non-dialysis patients. No significant correlations were found between IGF-1 or IGFBP-3 levels and growth rates or nutritional parameters. Thus growth retardation in children with CRF is not related to circulating levels of IGF-1 or IGFBP-3.
Url:
DOI: 10.1007/BF00874005
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ISTEX:1D65777BB2C52B097250457E313C800133A1C104Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Insulin-like growth factor-1, growth hormone-dependent insulin-like growth factor-binding protein and growth in children with chronic renal failure</title><author><name sortKey="Hodson, M" sort="Hodson, M" uniqKey="Hodson M" first="M." last="Hodson">M. Hodson</name><affiliation><mods:affiliation>Department of Paediatrics, Westmead Hospital, 2145, Westmead, New South Wales, Australia</mods:affiliation></affiliation></author><author><name sortKey="Brown, Shane" sort="Brown, Shane" uniqKey="Brown S" first="Shane" last="Brown">Shane Brown</name><affiliation><mods:affiliation>Department of Endocrinology, Prince of Wales Hospital, 2031, Randwick, New South Wales, Australia</mods:affiliation></affiliation></author><author><name sortKey="Roy, Paul" sort="Roy, Paul" uniqKey="Roy P" first="Paul" last="Roy">Paul Roy</name><affiliation><mods:affiliation>Department of Nephrology, Royal Alexandra Hospital for Children, 2050, Camperdown, New South Wales, Australia</mods:affiliation></affiliation></author><author><name sortKey="Rosenberg, R" sort="Rosenberg, R" uniqKey="Rosenberg R" first="R." last="Rosenberg">R. Rosenberg</name><affiliation><mods:affiliation>Department of Nephrology, Prince of Wales Children's Hospital, 2031, Randwick, New South Wales, Australia</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:1D65777BB2C52B097250457E313C800133A1C104</idno><date when="1992" year="1992">1992</date><idno type="doi">10.1007/BF00874005</idno><idno type="url">https://api.istex.fr/document/1D65777BB2C52B097250457E313C800133A1C104/fulltext/pdf</idno><idno type="wicri:Area/Main/Corpus">000A29</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Insulin-like growth factor-1, growth hormone-dependent insulin-like growth factor-binding protein and growth in children with chronic renal failure</title><author><name sortKey="Hodson, M" sort="Hodson, M" uniqKey="Hodson M" first="M." last="Hodson">M. Hodson</name><affiliation><mods:affiliation>Department of Paediatrics, Westmead Hospital, 2145, Westmead, New South Wales, Australia</mods:affiliation></affiliation></author><author><name sortKey="Brown, Shane" sort="Brown, Shane" uniqKey="Brown S" first="Shane" last="Brown">Shane Brown</name><affiliation><mods:affiliation>Department of Endocrinology, Prince of Wales Hospital, 2031, Randwick, New South Wales, Australia</mods:affiliation></affiliation></author><author><name sortKey="Roy, Paul" sort="Roy, Paul" uniqKey="Roy P" first="Paul" last="Roy">Paul Roy</name><affiliation><mods:affiliation>Department of Nephrology, Royal Alexandra Hospital for Children, 2050, Camperdown, New South Wales, Australia</mods:affiliation></affiliation></author><author><name sortKey="Rosenberg, R" sort="Rosenberg, R" uniqKey="Rosenberg R" first="R." last="Rosenberg">R. Rosenberg</name><affiliation><mods:affiliation>Department of Nephrology, Prince of Wales Children's Hospital, 2031, Randwick, New South Wales, Australia</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Pediatric Nephrology</title><title level="j" type="sub">Journal of the International Pediatric Nephrology Association</title><title level="j" type="abbrev">Pediatr Nephrol</title><idno type="ISSN">0931-041X</idno><idno type="eISSN">1432-198X</idno><imprint><publisher>Springer-Verlag</publisher><pubPlace>Berlin/Heidelberg</pubPlace><date type="published" when="1992-09-01">1992-09-01</date><biblScope unit="volume">6</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="433">433</biblScope><biblScope unit="page" to="438">438</biblScope></imprint><idno type="ISSN">0931-041X</idno></series><idno type="istex">1D65777BB2C52B097250457E313C800133A1C104</idno><idno type="DOI">10.1007/BF00874005</idno><idno type="ArticleID">Art12</idno><idno type="ArticleID">BF00874005</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0931-041X</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: Insulin-like growth factor-binding protein-3 (IGFBP-3) and insulin-like growth factor-1 (IGF-1) levels were measured by specific radioimmunoassays in children with all degrees of chronic renal failure (CRF). Study group 1 comprised 29 children (10 on dialysis) who had been studied one to four times over 2 years to determine whether IGF-1 and IGFBP-3 levels differed from those in age-matched healthy children and to examine the relationship between these levels and heights. IGF-1 and IGFBP-3 levels did not differ from those in normal children. IGF-1 and IGFBP-3 were significantly correlated, increased with pubertal stage in all children and with age in non-dialysis patients. IGF-1, but not IGFBP-3, correlated with age in dialysis patients. There was no correlation between IGF-1 or IGFBP-3 levels (corrected for age) and height standard deviation score (SDS) in either non-dialysis or dialysis patients. Study group 2 comprised 19 children (7 on dialysis) who were studied prospectively for 1–2 years to examine the relationship between IGF-1 and IGFBP-3 levels, growth rates and nutritional parameters. Mean values of IGF-1 and IGFBP-3 (corrected for age) did not change over 1-year periods, while height SDS fell by −0.38 ±0.21 SD/year in dialysis patients and by −0.11 ±0.29 SD/year in non-dialysis patients. No significant correlations were found between IGF-1 or IGFBP-3 levels and growth rates or nutritional parameters. Thus growth retardation in children with CRF is not related to circulating levels of IGF-1 or IGFBP-3.</div></front></TEI><istex><corpusName>springer</corpusName><author><json:item><name>Elisabeth M. Hodson</name><affiliations><json:string>Department of Paediatrics, Westmead Hospital, 2145, Westmead, New South Wales, Australia</json:string></affiliations></json:item><json:item><name>A. Shane Brown</name><affiliations><json:string>Department of Endocrinology, Prince of Wales Hospital, 2031, Randwick, New South Wales, Australia</json:string></affiliations></json:item><json:item><name>L. Paul Roy</name><affiliations><json:string>Department of Nephrology, Royal Alexandra Hospital for Children, 2050, Camperdown, New South Wales, Australia</json:string></affiliations></json:item><json:item><name>Andrew R. Rosenberg</name><affiliations><json:string>Department of Nephrology, Prince of Wales Children's Hospital, 2031, Randwick, New South Wales, Australia</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Insulin-like growth factor-1</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Insulin-like growth factor-binding protein-3</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Chronic renal failure</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Growth retardation</value></json:item></subject><language><json:string>eng</json:string></language><abstract>Abstract: Insulin-like growth factor-binding protein-3 (IGFBP-3) and insulin-like growth factor-1 (IGF-1) levels were measured by specific radioimmunoassays in children with all degrees of chronic renal failure (CRF). Study group 1 comprised 29 children (10 on dialysis) who had been studied one to four times over 2 years to determine whether IGF-1 and IGFBP-3 levels differed from those in age-matched healthy children and to examine the relationship between these levels and heights. IGF-1 and IGFBP-3 levels did not differ from those in normal children. IGF-1 and IGFBP-3 were significantly correlated, increased with pubertal stage in all children and with age in non-dialysis patients. IGF-1, but not IGFBP-3, correlated with age in dialysis patients. There was no correlation between IGF-1 or IGFBP-3 levels (corrected for age) and height standard deviation score (SDS) in either non-dialysis or dialysis patients. Study group 2 comprised 19 children (7 on dialysis) who were studied prospectively for 1–2 years to examine the relationship between IGF-1 and IGFBP-3 levels, growth rates and nutritional parameters. Mean values of IGF-1 and IGFBP-3 (corrected for age) did not change over 1-year periods, while height SDS fell by −0.38 ±0.21 SD/year in dialysis patients and by −0.11 ±0.29 SD/year in non-dialysis patients. No significant correlations were found between IGF-1 or IGFBP-3 levels and growth rates or nutritional parameters. 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Study group 1 comprised 29 children (10 on dialysis) who had been studied one to four times over 2 years to determine whether IGF-1 and IGFBP-3 levels differed from those in age-matched healthy children and to examine the relationship between these levels and heights. IGF-1 and IGFBP-3 levels did not differ from those in normal children. IGF-1 and IGFBP-3 were significantly correlated, increased with pubertal stage in all children and with age in non-dialysis patients. IGF-1, but not IGFBP-3, correlated with age in dialysis patients. There was no correlation between IGF-1 or IGFBP-3 levels (corrected for age) and height standard deviation score (SDS) in either non-dialysis or dialysis patients. Study group 2 comprised 19 children (7 on dialysis) who were studied prospectively for 1–2 years to examine the relationship between IGF-1 and IGFBP-3 levels, growth rates and nutritional parameters. Mean values of IGF-1 and IGFBP-3 (corrected for age) did not change over 1-year periods, while height SDS fell by −0.38 ±0.21 SD/year in dialysis patients and by −0.11 ±0.29 SD/year in non-dialysis patients. No significant correlations were found between IGF-1 or IGFBP-3 levels and growth rates or nutritional parameters. Thus growth retardation in children with CRF is not related to circulating levels of IGF-1 or IGFBP-3.</p></abstract><textClass><keywords scheme="Journal Subject"><list><head>Medicine & Public Health</head><item><term>Pediatrics</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1991-07-26">Created</change><change when="1992-09-01">Published</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2016-3-1">References added</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/1D65777BB2C52B097250457E313C800133A1C104/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Springer, Publisher found" wicri:toSee="no header"><istex:xmlDeclaration>version="1.0" encoding="UTF-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//Springer-Verlag//DTD A++ V2.4//EN" 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TocLevels="0"><VolumeIDStart>6</VolumeIDStart><VolumeIDEnd>6</VolumeIDEnd><VolumeIssueCount>6</VolumeIssueCount></VolumeInfo><Issue IssueType="Regular"><IssueInfo TocLevels="0"><IssueIDStart>5</IssueIDStart><IssueIDEnd>5</IssueIDEnd><IssueArticleCount>33</IssueArticleCount><IssueHistory><CoverDate><Year>1992</Year><Month>9</Month></CoverDate></IssueHistory><IssueCopyright><CopyrightHolderName>IPNA</CopyrightHolderName><CopyrightYear>1992</CopyrightYear></IssueCopyright></IssueInfo><Article ID="Art12"><ArticleInfo Language="En" ArticleType="OriginalPaper" NumberingStyle="Unnumbered" TocLevels="0" ContainsESM="No"><ArticleID>BF00874005</ArticleID><ArticleDOI>10.1007/BF00874005</ArticleDOI><ArticleSequenceNumber>12</ArticleSequenceNumber><ArticleTitle Language="En">Insulin-like growth factor-1, growth hormone-dependent insulin-like growth factor-binding protein and growth in children with chronic renal failure</ArticleTitle><ArticleCategory>Original Article</ArticleCategory><ArticleFirstPage>433</ArticleFirstPage><ArticleLastPage>438</ArticleLastPage><ArticleHistory><RegistrationDate><Year>2004</Year><Month>12</Month><Day>8</Day></RegistrationDate><Received><Year>1991</Year><Month>7</Month><Day>26</Day></Received><Revised><Year>1991</Year><Month>12</Month><Day>17</Day></Revised><Accepted><Year>1992</Year><Month>1</Month><Day>9</Day></Accepted></ArticleHistory><ArticleCopyright><CopyrightHolderName>IPNA</CopyrightHolderName><CopyrightYear>1992</CopyrightYear></ArticleCopyright><ArticleGrants Type="Regular"><MetadataGrant Grant="OpenAccess"></MetadataGrant><AbstractGrant Grant="OpenAccess"></AbstractGrant><BodyPDFGrant Grant="Restricted"></BodyPDFGrant><BodyHTMLGrant Grant="Restricted"></BodyHTMLGrant><BibliographyGrant Grant="Restricted"></BibliographyGrant><ESMGrant Grant="Restricted"></ESMGrant></ArticleGrants><ArticleContext><JournalID>467</JournalID><VolumeIDStart>6</VolumeIDStart><VolumeIDEnd>6</VolumeIDEnd><IssueIDStart>5</IssueIDStart><IssueIDEnd>5</IssueIDEnd></ArticleContext></ArticleInfo><ArticleHeader><AuthorGroup><Author AffiliationIDS="Aff1" CorrespondingAffiliationID="Aff1"><AuthorName DisplayOrder="Western"><GivenName>Elisabeth</GivenName><GivenName>M.</GivenName><FamilyName>Hodson</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff2"><AuthorName DisplayOrder="Western"><GivenName>A.</GivenName><GivenName>Shane</GivenName><FamilyName>Brown</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff3"><AuthorName DisplayOrder="Western"><GivenName>L.</GivenName><GivenName>Paul</GivenName><FamilyName>Roy</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff4"><AuthorName DisplayOrder="Western"><GivenName>Andrew</GivenName><GivenName>R.</GivenName><FamilyName>Rosenberg</FamilyName></AuthorName></Author><Affiliation ID="Aff1"><OrgDivision>Department of Paediatrics</OrgDivision><OrgName>Westmead Hospital</OrgName><OrgAddress><Postcode>2145</Postcode><City>Westmead</City><State>New South Wales</State><Country>Australia</Country></OrgAddress></Affiliation><Affiliation ID="Aff2"><OrgDivision>Department of Endocrinology</OrgDivision><OrgName>Prince of Wales Hospital</OrgName><OrgAddress><Postcode>2031</Postcode><City>Randwick</City><State>New South Wales</State><Country>Australia</Country></OrgAddress></Affiliation><Affiliation ID="Aff3"><OrgDivision>Department of Nephrology</OrgDivision><OrgName>Royal Alexandra Hospital for Children</OrgName><OrgAddress><Postcode>2050</Postcode><City>Camperdown</City><State>New South Wales</State><Country>Australia</Country></OrgAddress></Affiliation><Affiliation ID="Aff4"><OrgDivision>Department of Nephrology</OrgDivision><OrgName>Prince of Wales Children's Hospital</OrgName><OrgAddress><Postcode>2031</Postcode><City>Randwick</City><State>New South Wales</State><Country>Australia</Country></OrgAddress></Affiliation></AuthorGroup><Abstract ID="Abs1" Language="En"><Heading>Abstract</Heading><Para>Insulin-like growth factor-binding protein-3 (IGFBP-3) and insulin-like growth factor-1 (IGF-1) levels were measured by specific radioimmunoassays in children with all degrees of chronic renal failure (CRF). Study group 1 comprised 29 children (10 on dialysis) who had been studied one to four times over 2 years to determine whether IGF-1 and IGFBP-3 levels differed from those in age-matched healthy children and to examine the relationship between these levels and heights. IGF-1 and IGFBP-3 levels did not differ from those in normal children. IGF-1 and IGFBP-3 were significantly correlated, increased with pubertal stage in all children and with age in non-dialysis patients. IGF-1, but not IGFBP-3, correlated with age in dialysis patients. There was no correlation between IGF-1 or IGFBP-3 levels (corrected for age) and height standard deviation score (SDS) in either non-dialysis or dialysis patients. Study group 2 comprised 19 children (7 on dialysis) who were studied prospectively for 1–2 years to examine the relationship between IGF-1 and IGFBP-3 levels, growth rates and nutritional parameters. Mean values of IGF-1 and IGFBP-3 (corrected for age) did not change over 1-year periods, while height SDS fell by −0.38 ±0.21 SD/year in dialysis patients and by −0.11 ±0.29 SD/year in non-dialysis patients. No significant correlations were found between IGF-1 or IGFBP-3 levels and growth rates or nutritional parameters. Thus growth retardation in children with CRF is not related to circulating levels of IGF-1 or IGFBP-3.</Para></Abstract><KeywordGroup Language="En"><Heading>Key words</Heading><Keyword>Insulin-like growth factor-1</Keyword><Keyword>Insulin-like growth factor-binding protein-3</Keyword><Keyword>Chronic renal failure</Keyword><Keyword>Growth retardation</Keyword></KeywordGroup></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Insulin-like growth factor-1, growth hormone-dependent insulin-like growth factor-binding protein and growth in children with chronic renal failure</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Insulin-like growth factor-1, growth hormone-dependent insulin-like growth factor-binding protein and growth in children with chronic renal failure</title></titleInfo><name type="personal" displayLabel="corresp"><namePart type="given">Elisabeth</namePart><namePart type="given">M.</namePart><namePart type="family">Hodson</namePart><affiliation>Department of Paediatrics, Westmead Hospital, 2145, Westmead, New South Wales, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A.</namePart><namePart type="given">Shane</namePart><namePart type="family">Brown</namePart><affiliation>Department of Endocrinology, Prince of Wales Hospital, 2031, Randwick, New South Wales, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">L.</namePart><namePart type="given">Paul</namePart><namePart type="family">Roy</namePart><affiliation>Department of Nephrology, Royal Alexandra Hospital for Children, 2050, Camperdown, New South Wales, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Andrew</namePart><namePart type="given">R.</namePart><namePart type="family">Rosenberg</namePart><affiliation>Department of Nephrology, Prince of Wales Children's Hospital, 2031, Randwick, New South Wales, Australia</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="OriginalPaper"></genre><originInfo><publisher>Springer-Verlag</publisher><place><placeTerm type="text">Berlin/Heidelberg</placeTerm></place><dateCreated encoding="w3cdtf">1991-07-26</dateCreated><dateIssued encoding="w3cdtf">1992-09-01</dateIssued><copyrightDate encoding="w3cdtf">1992</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Abstract: Insulin-like growth factor-binding protein-3 (IGFBP-3) and insulin-like growth factor-1 (IGF-1) levels were measured by specific radioimmunoassays in children with all degrees of chronic renal failure (CRF). Study group 1 comprised 29 children (10 on dialysis) who had been studied one to four times over 2 years to determine whether IGF-1 and IGFBP-3 levels differed from those in age-matched healthy children and to examine the relationship between these levels and heights. IGF-1 and IGFBP-3 levels did not differ from those in normal children. IGF-1 and IGFBP-3 were significantly correlated, increased with pubertal stage in all children and with age in non-dialysis patients. IGF-1, but not IGFBP-3, correlated with age in dialysis patients. There was no correlation between IGF-1 or IGFBP-3 levels (corrected for age) and height standard deviation score (SDS) in either non-dialysis or dialysis patients. Study group 2 comprised 19 children (7 on dialysis) who were studied prospectively for 1–2 years to examine the relationship between IGF-1 and IGFBP-3 levels, growth rates and nutritional parameters. Mean values of IGF-1 and IGFBP-3 (corrected for age) did not change over 1-year periods, while height SDS fell by −0.38 ±0.21 SD/year in dialysis patients and by −0.11 ±0.29 SD/year in non-dialysis patients. No significant correlations were found between IGF-1 or IGFBP-3 levels and growth rates or nutritional parameters. Thus growth retardation in children with CRF is not related to circulating levels of IGF-1 or IGFBP-3.</abstract><note>Original Article</note><relatedItem type="host"><titleInfo><title>Pediatric Nephrology</title><subTitle>Journal of the International Pediatric Nephrology Association</subTitle></titleInfo><titleInfo type="abbreviated"><title>Pediatr Nephrol</title></titleInfo><genre type="Journal" displayLabel="Archive Journal"></genre><originInfo><dateIssued encoding="w3cdtf">1992-09-01</dateIssued><copyrightDate encoding="w3cdtf">1992</copyrightDate></originInfo><subject><genre>Medicine & Public Health</genre><topic>Pediatrics</topic></subject><identifier type="ISSN">0931-041X</identifier><identifier type="eISSN">1432-198X</identifier><identifier type="JournalID">467</identifier><identifier type="IssueArticleCount">33</identifier><identifier type="VolumeIssueCount">6</identifier><part><date>1992</date><detail type="volume"><number>6</number><caption>vol.</caption></detail><detail type="issue"><number>5</number><caption>no.</caption></detail><extent unit="pages"><start>433</start><end>438</end></extent></part><recordInfo><recordOrigin>IPNA, 1992</recordOrigin></recordInfo></relatedItem><identifier type="istex">1D65777BB2C52B097250457E313C800133A1C104</identifier><identifier type="DOI">10.1007/BF00874005</identifier><identifier type="ArticleID">Art12</identifier><identifier type="ArticleID">BF00874005</identifier><accessCondition type="use and reproduction" contentType="copyright">IPNA</accessCondition><recordInfo><recordContentSource>SPRINGER</recordContentSource><recordOrigin>IPNA, 1992</recordOrigin></recordInfo></mods></metadata><enrichments><istex:refBibTEI uri="https://api.istex.fr/document/1D65777BB2C52B097250457E313C800133A1C104/enrichments/refBib"><teiHeader></teiHeader><text><front></front><body></body><back><listBibl><biblStruct xml:id="b0"><analytic><title level="a" type="main">End stage renal failure in children: 16 years' experience at one Australian Centre</title><author><persName><forename type="first">Em</forename><surname>Hodson</surname></persName></author><author><persName><forename type="first">Jf</forename><surname>Knight</surname></persName></author><author><persName><forename type="first">Agr</forename><surname>Sheil</surname></persName></author><author><persName><forename type="first">Lp</forename><surname>Roy</surname></persName></author><author><persName><forename type="first">Jp</forename><surname>Harris</surname></persName></author><author><persName><forename type="first">Jr</forename><surname>Rogers</surname></persName></author><author><persName><forename type="first">Ms</forename><surname>Stephen</surname></persName></author><author><persName><forename type="first">J</forename><surname>Boulas</surname></persName></author><author><persName><forename type="first">Jf</forename><surname>Thompson</surname></persName></author></analytic><monogr><title level="j">Med J Aust</title><imprint><biblScope unit="volume">152</biblScope><biblScope unit="page" from="245" to="250"></biblScope><date type="published" when="1990"></date></imprint></monogr></biblStruct><biblStruct xml:id="b1"><analytic><title level="a" type="main">Growth and metabolism in renal failure. 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Babies with dilated renal collecting systems underwent further investigations (micturating cystourethrography, intravenous urography, or radioisotope study) With these methods, 11 children were found to have renal disorders . A postal follow-up survey was carried out when the children were 3 years old. 657 (62%) families responded. We searched for non-responders among children born in 1986 who had subsequently had a renal S. Matthews radioisotope investigation: 5 non-responders were found among these children. Of the total, 24 children had had a urinary-tract infection: 3 more children with ureteric reflux were found; their neonatal ultrasound scans had suggested no abnormality. Thus, more than half the children of this cohort in whom hydronephrosis or ureteric reflux developed had only slight dilatation (less than 5 mm) on the neonatal scan. On review of the original videotapes there was no difference in internal dimension between left and right kidneys: the internal dimension was 5 mm or less in both kidneys in 96.3% of babies and 4 mm or less in 93</title><author><persName><forename type="first">J</forename><forename type="middle">E S</forename><surname>Scott</surname></persName></author><author><persName><forename type="first">R</forename><forename type="middle">E J</forename><surname>Lee</surname></persName></author><author><persName><forename type="first">E</forename><forename type="middle">W</forename><surname>Hunter</surname></persName></author><author><persName><forename type="first">M</forename><forename type="middle">G</forename><surname>Coulthard</surname></persName></author><author><persName><forename type="first">J</forename><forename type="middle">N</forename></persName></author><imprint></imprint></monogr></biblStruct></listBibl></back></text></istex:refBibTEI></enrichments><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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