Non-HLA-linked hemochromatosis in a Chinese woman
Identifieur interne : 003E54 ( Istex/Corpus ); précédent : 003E53; suivant : 003E55Non-HLA-linked hemochromatosis in a Chinese woman
Auteurs : Matt Oliver ; Linda Scully ; Colette Guiraudon ; C. AdamsSource :
- Digestive Diseases and Sciences [ 0163-2116 ] ; 1995-07-01.
Abstract
Summary: A 55-year-old Chinese woman is described with severe iron overload similar in degree and distribution to that seen in hereditary hemochromatosis in the Causasian population. Autopsy findings confirmed severe iron overload in the liver, pancreases, skin, heart, and endocrine organs. Hepatic iron concentration was 482 μmol/g with a hepatic iron index of 8.8. There was no history of thalassemia, transfusions, or alcohol abuse. Pedigree analysis revealed two HLA identical brothers that had no clinical or biochemical evidence of iron overload. This case is an unsual example of severe iron overload in a non-Causasian kindred and may represent a non-HLA-linked form of iron overload.
Url:
DOI: 10.1007/BF02285215
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Adams</name><affiliation><mods:affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:DE6C70E154CAAE6A594E22E8E623E640A051D6DF</idno><date when="1995" year="1995">1995</date><idno type="doi">10.1007/BF02285215</idno><idno type="url">https://api.istex.fr/document/DE6C70E154CAAE6A594E22E8E623E640A051D6DF/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">003E54</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Non-HLA-linked hemochromatosis in a Chinese woman</title><author><name sortKey="Oliver, Matt" sort="Oliver, Matt" uniqKey="Oliver M" first="Matt" last="Oliver">Matt Oliver</name><affiliation><mods:affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</mods:affiliation></affiliation></author><author><name sortKey="Scully, Linda" sort="Scully, Linda" uniqKey="Scully L" first="Linda" last="Scully">Linda Scully</name><affiliation><mods:affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</mods:affiliation></affiliation></author><author><name sortKey="Guiraudon, Colette" sort="Guiraudon, Colette" uniqKey="Guiraudon C" first="Colette" last="Guiraudon">Colette Guiraudon</name><affiliation><mods:affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</mods:affiliation></affiliation></author><author><name sortKey="Adams, C" sort="Adams, C" uniqKey="Adams C" first="C." last="Adams">C. Adams</name><affiliation><mods:affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Digestive Diseases and Sciences</title><title level="j" type="abbrev">Digest Dis Sci</title><idno type="ISSN">0163-2116</idno><idno type="eISSN">1573-2568</idno><imprint><publisher>Kluwer Academic Publishers-Plenum Publishers</publisher><pubPlace>New York</pubPlace><date type="published" when="1995-07-01">1995-07-01</date><biblScope unit="volume">40</biblScope><biblScope unit="issue">7</biblScope><biblScope unit="page" from="1589">1589</biblScope><biblScope unit="page" to="1591">1591</biblScope></imprint><idno type="ISSN">0163-2116</idno></series><idno type="istex">DE6C70E154CAAE6A594E22E8E623E640A051D6DF</idno><idno type="DOI">10.1007/BF02285215</idno><idno type="ArticleID">BF02285215</idno><idno type="ArticleID">Art32</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0163-2116</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Summary: A 55-year-old Chinese woman is described with severe iron overload similar in degree and distribution to that seen in hereditary hemochromatosis in the Causasian population. Autopsy findings confirmed severe iron overload in the liver, pancreases, skin, heart, and endocrine organs. Hepatic iron concentration was 482 μmol/g with a hepatic iron index of 8.8. There was no history of thalassemia, transfusions, or alcohol abuse. Pedigree analysis revealed two HLA identical brothers that had no clinical or biochemical evidence of iron overload. This case is an unsual example of severe iron overload in a non-Causasian kindred and may represent a non-HLA-linked form of iron overload.</div></front></TEI><istex><corpusName>springer</corpusName><author><json:item><name>Matt Oliver MD</name><affiliations><json:string>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</json:string><json:string>Department of Medicine, University of Ottawa, Ottawa, Canada</json:string></affiliations></json:item><json:item><name>Linda Scully MD</name><affiliations><json:string>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</json:string><json:string>Department of Medicine, University of Ottawa, Ottawa, Canada</json:string></affiliations></json:item><json:item><name>Colette Guiraudon MD</name><affiliations><json:string>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</json:string><json:string>Department of Medicine, University of Ottawa, Ottawa, Canada</json:string></affiliations></json:item><json:item><name>Dr. Paul C. Adams MD</name><affiliations><json:string>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</json:string><json:string>Department of Medicine, University of Ottawa, Ottawa, Canada</json:string></affiliations></json:item></author><articleId><json:string>BF02285215</json:string><json:string>Art32</json:string></articleId><language><json:string>eng</json:string></language><abstract>Summary: A 55-year-old Chinese woman is described with severe iron overload similar in degree and distribution to that seen in hereditary hemochromatosis in the Causasian population. Autopsy findings confirmed severe iron overload in the liver, pancreases, skin, heart, and endocrine organs. Hepatic iron concentration was 482 μmol/g with a hepatic iron index of 8.8. There was no history of thalassemia, transfusions, or alcohol abuse. Pedigree analysis revealed two HLA identical brothers that had no clinical or biochemical evidence of iron overload. 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Medicine and Pathology, University of Western Ontario, London, Ontario</affiliation><affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</affiliation></author><author><persName><forename type="first">Linda</forename><surname>Scully</surname></persName><roleName type="degree">MD</roleName><affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</affiliation><affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</affiliation></author><author><persName><forename type="first">Colette</forename><surname>Guiraudon</surname></persName><roleName type="degree">MD</roleName><affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</affiliation><affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</affiliation></author><author corresp="yes"><persName><forename type="first">Paul</forename><surname>Adams</surname></persName><roleName 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ContainsESM="No"><ArticleID>BF02285215</ArticleID><ArticleDOI>10.1007/BF02285215</ArticleDOI><ArticleSequenceNumber>32</ArticleSequenceNumber><ArticleTitle Language="En">Non-HLA-linked hemochromatosis in a Chinese woman</ArticleTitle><ArticleCategory>Liver: Infectious, Inflammatory, and Metabolic Disorders</ArticleCategory><ArticleSubCategory>Case Report</ArticleSubCategory><ArticleFirstPage>1589</ArticleFirstPage><ArticleLastPage>1591</ArticleLastPage><ArticleHistory><RegistrationDate><Year>2005</Year><Month>12</Month><Day>9</Day></RegistrationDate><Received><Year>1994</Year><Month>10</Month><Day>17</Day></Received><Revised><Year>1995</Year><Month>2</Month><Day>7</Day></Revised><Accepted><Year>1995</Year><Month>3</Month><Day>27</Day></Accepted></ArticleHistory><ArticleCopyright><CopyrightHolderName>Plenum Publishing Corporation</CopyrightHolderName><CopyrightYear>1995</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>10620</JournalID><VolumeIDStart>40</VolumeIDStart><VolumeIDEnd>40</VolumeIDEnd><IssueIDStart>7</IssueIDStart><IssueIDEnd>7</IssueIDEnd></ArticleContext></ArticleInfo><ArticleHeader><AuthorGroup><Author AffiliationIDS="Aff1 Aff2"><AuthorName DisplayOrder="Western"><GivenName>Matt</GivenName><FamilyName>Oliver</FamilyName><Degrees>MD</Degrees></AuthorName></Author><Author AffiliationIDS="Aff1 Aff2"><AuthorName DisplayOrder="Western"><GivenName>Linda</GivenName><FamilyName>Scully</FamilyName><Degrees>MD</Degrees></AuthorName></Author><Author AffiliationIDS="Aff1 Aff2"><AuthorName DisplayOrder="Western"><GivenName>Colette</GivenName><FamilyName>Guiraudon</FamilyName><Degrees>MD</Degrees></AuthorName></Author><Author AffiliationIDS="Aff1 Aff2" CorrespondingAffiliationID="Aff3"><AuthorName DisplayOrder="Western"><Prefix>Dr.</Prefix><GivenName>Paul</GivenName><GivenName>C.</GivenName><FamilyName>Adams</FamilyName><Degrees>MD</Degrees></AuthorName></Author><Affiliation ID="Aff1"><OrgDivision>Departments of Medicine and Pathology</OrgDivision><OrgName>University of Western Ontario</OrgName><OrgAddress><City>London</City><State>Ontario</State></OrgAddress></Affiliation><Affiliation ID="Aff2"><OrgDivision>Department of Medicine</OrgDivision><OrgName>University of Ottawa</OrgName><OrgAddress><City>Ottawa</City><Country>Canada</Country></OrgAddress></Affiliation><Affiliation ID="Aff3"><OrgDivision>Department of Medicine</OrgDivision><OrgName>University Hospital</OrgName><OrgAddress><Street>339 Windermere Rd.</Street><Postbox>P.O. Box 5339</Postbox><Postcode>N6A 5A5</Postcode><City>London</City><State>Ontario</State><Country>Canada</Country></OrgAddress></Affiliation></AuthorGroup><Abstract ID="Abs1" Language="En"><Heading>Summary</Heading><Para>A 55-year-old Chinese woman is described with severe iron overload similar in degree and distribution to that seen in hereditary hemochromatosis in the Causasian population. Autopsy findings confirmed severe iron overload in the liver, pancreases, skin, heart, and endocrine organs. Hepatic iron concentration was 482 μmol/g with a hepatic iron index of 8.8. There was no history of thalassemia, transfusions, or alcohol abuse. Pedigree analysis revealed two HLA identical brothers that had no clinical or biochemical evidence of iron overload. This case is an unsual example of severe iron overload in a non-Causasian kindred and may represent a non-HLA-linked form of iron overload.</Para></Abstract><KeywordGroup Language="En"><Heading>Key Words</Heading><Keyword>non-HLA-linked hemochromatosis</Keyword><Keyword>Chinese</Keyword></KeywordGroup></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Non-HLA-linked hemochromatosis in a Chinese woman</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Non-HLA-linked hemochromatosis in a Chinese woman</title></titleInfo><name type="personal"><namePart type="given">Matt</namePart><namePart type="family">Oliver</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</affiliation><affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Linda</namePart><namePart type="family">Scully</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</affiliation><affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Colette</namePart><namePart type="family">Guiraudon</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</affiliation><affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal" displayLabel="corresp"><namePart type="termsOfAddress">Dr.</namePart><namePart type="given">Paul</namePart><namePart type="given">C.</namePart><namePart type="family">Adams</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Departments of Medicine and Pathology, University of Western Ontario, London, Ontario</affiliation><affiliation>Department of Medicine, University of Ottawa, Ottawa, Canada</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="OriginalPaper"></genre><originInfo><publisher>Kluwer Academic Publishers-Plenum Publishers</publisher><place><placeTerm type="text">New York</placeTerm></place><dateCreated encoding="w3cdtf">1994-10-17</dateCreated><dateIssued encoding="w3cdtf">1995-07-01</dateIssued><copyrightDate encoding="w3cdtf">1995</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">Summary: A 55-year-old Chinese woman is described with severe iron overload similar in degree and distribution to that seen in hereditary hemochromatosis in the Causasian population. Autopsy findings confirmed severe iron overload in the liver, pancreases, skin, heart, and endocrine organs. Hepatic iron concentration was 482 μmol/g with a hepatic iron index of 8.8. There was no history of thalassemia, transfusions, or alcohol abuse. Pedigree analysis revealed two HLA identical brothers that had no clinical or biochemical evidence of iron overload. 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