ARTICLE: Axenfeld–Rieger Syndrome (ARS): A review and case report
Identifieur interne : 000C64 ( Istex/Corpus ); précédent : 000C63; suivant : 000C65ARTICLE: Axenfeld–Rieger Syndrome (ARS): A review and case report
Auteurs : Jennie M. Waldron ; Clare Mcnamara ; Antonia R. Hewson ; C. M. McnamaraSource :
- Special Care in Dentistry [ 0275-1879 ] ; 2010-09.
English descriptors
- KwdEn :
- Abnormality, Anomaly, Anterior chamber, Axenfeld syndrome, Bone density, Case report, Community services, Craniofacial, Craniofacial features, Dental anomalies, Dental department, Dental literature, Dental management, Dietary advice, Family history, First molar, Gingival maturation, Hypodontia, Hypoplasia, Incisor, Little information, Mandibular, Mandibular teeth, Maxillary, Maxillary hypodontia, Midface hypoplasia, Molar, Multidisciplinary approach, Neural crest cells, Ocular, Ocular features, Orthodontic treatment, Osteopenia, Osteoporosis, Partial denture, Periodontal disease, Periumbilical skin, Restorative care, Rieger syndrome, Secondary teeth, Somatic anomalies, Syndrome, Wide variety.
- Teeft :
- Abnormality, Anomaly, Anterior chamber, Axenfeld syndrome, Bone density, Case report, Community services, Craniofacial, Craniofacial features, Dental anomalies, Dental department, Dental literature, Dental management, Dietary advice, Family history, First molar, Gingival maturation, Hypodontia, Hypoplasia, Incisor, Little information, Mandibular, Mandibular teeth, Maxillary, Maxillary hypodontia, Midface hypoplasia, Molar, Multidisciplinary approach, Neural crest cells, Ocular, Ocular features, Orthodontic treatment, Osteopenia, Osteoporosis, Partial denture, Periodontal disease, Periumbilical skin, Restorative care, Rieger syndrome, Secondary teeth, Somatic anomalies, Syndrome, Wide variety.
Abstract
Axenfeld–Rieger syndrome (ARS) is a rare, autosomal dominant condition characterized by ocular, craniofacial, dental, and periumbilical abnormalities. Relatively little information exists on this syndrome within the dental literature despite the fact that midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome. This is a case report of a 7‐year‐old Caucasian female with ARS who presented with significant ocular and dental anomalies. She was also found to have osteopenia. Her dental condition is described, her immediate treatment is shown, and her long‐term treatment needs are discussed.
Url:
DOI: 10.1111/j.1754-4505.2010.00153.x
Links to Exploration step
ISTEX:19B54ABF9FCB8E102A14D8121D5A5598C0285A67Le document en format XML
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Waldron</name><affiliation><mods:affiliation>Vocational Trainee, Dental Department, Community Services, Mayo, Ireland</mods:affiliation></affiliation></author><author><name sortKey="Mcnamara, Clare" sort="Mcnamara, Clare" uniqKey="Mcnamara C" first="Clare" last="Mcnamara">Clare Mcnamara</name><affiliation><mods:affiliation>Senior Registrar, Department of Orthodontics, Gloucester Royal Hospital, Gloucestershire, UK</mods:affiliation></affiliation></author><author><name sortKey="Hewson, Antonia R" sort="Hewson, Antonia R" uniqKey="Hewson A" first="Antonia R." last="Hewson">Antonia R. Hewson</name><affiliation><mods:affiliation>Principal Dental Surgeon, Dental Department, Community Services, Mayo, Ireland</mods:affiliation></affiliation></author><author><name sortKey="Mcnamara, C M" sort="Mcnamara, C M" uniqKey="Mcnamara C" first="C. M." last="Mcnamara">C. M. Mcnamara</name><affiliation><mods:affiliation>Consultant Orthodontist, HSE, Ireland.</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: triona.mcnamara@gmail.com</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Special Care in Dentistry</title><title level="j" type="alt">SPECIAL CARE IN DENTISTRY</title><idno type="ISSN">0275-1879</idno><idno type="eISSN">1754-4505</idno><imprint><biblScope unit="vol">30</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="218">218</biblScope><biblScope unit="page" to="222">222</biblScope><biblScope unit="page-count">5</biblScope><publisher>Blackwell Publishing Inc</publisher><pubPlace>Malden, USA</pubPlace><date type="published" when="2010-09">2010-09</date></imprint><idno type="ISSN">0275-1879</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0275-1879</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Abnormality</term><term>Anomaly</term><term>Anterior chamber</term><term>Axenfeld syndrome</term><term>Bone density</term><term>Case report</term><term>Community services</term><term>Craniofacial</term><term>Craniofacial features</term><term>Dental anomalies</term><term>Dental department</term><term>Dental literature</term><term>Dental management</term><term>Dietary advice</term><term>Family history</term><term>First molar</term><term>Gingival maturation</term><term>Hypodontia</term><term>Hypoplasia</term><term>Incisor</term><term>Little information</term><term>Mandibular</term><term>Mandibular teeth</term><term>Maxillary</term><term>Maxillary hypodontia</term><term>Midface hypoplasia</term><term>Molar</term><term>Multidisciplinary approach</term><term>Neural crest cells</term><term>Ocular</term><term>Ocular features</term><term>Orthodontic treatment</term><term>Osteopenia</term><term>Osteoporosis</term><term>Partial denture</term><term>Periodontal disease</term><term>Periumbilical skin</term><term>Restorative care</term><term>Rieger syndrome</term><term>Secondary teeth</term><term>Somatic anomalies</term><term>Syndrome</term><term>Wide variety</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Abnormality</term><term>Anomaly</term><term>Anterior chamber</term><term>Axenfeld syndrome</term><term>Bone density</term><term>Case report</term><term>Community services</term><term>Craniofacial</term><term>Craniofacial features</term><term>Dental anomalies</term><term>Dental department</term><term>Dental literature</term><term>Dental management</term><term>Dietary advice</term><term>Family history</term><term>First molar</term><term>Gingival maturation</term><term>Hypodontia</term><term>Hypoplasia</term><term>Incisor</term><term>Little information</term><term>Mandibular</term><term>Mandibular teeth</term><term>Maxillary</term><term>Maxillary hypodontia</term><term>Midface hypoplasia</term><term>Molar</term><term>Multidisciplinary approach</term><term>Neural crest cells</term><term>Ocular</term><term>Ocular features</term><term>Orthodontic treatment</term><term>Osteopenia</term><term>Osteoporosis</term><term>Partial denture</term><term>Periodontal disease</term><term>Periumbilical skin</term><term>Restorative care</term><term>Rieger syndrome</term><term>Secondary teeth</term><term>Somatic anomalies</term><term>Syndrome</term><term>Wide variety</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Axenfeld–Rieger syndrome (ARS) is a rare, autosomal dominant condition characterized by ocular, craniofacial, dental, and periumbilical abnormalities. Relatively little information exists on this syndrome within the dental literature despite the fact that midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome. This is a case report of a 7‐year‐old Caucasian female with ARS who presented with significant ocular and dental anomalies. She was also found to have osteopenia. Her dental condition is described, her immediate treatment is shown, and her long‐term treatment needs are discussed.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>maxillary</json:string><json:string>osteopenia</json:string><json:string>mandibular</json:string><json:string>hypoplasia</json:string><json:string>craniofacial</json:string><json:string>incisor</json:string><json:string>abnormality</json:string><json:string>hypodontia</json:string><json:string>anomaly</json:string><json:string>syndrome</json:string><json:string>molar</json:string><json:string>midface hypoplasia</json:string><json:string>rieger syndrome</json:string><json:string>dental anomalies</json:string><json:string>multidisciplinary approach</json:string><json:string>secondary teeth</json:string><json:string>osteoporosis</json:string><json:string>case report</json:string><json:string>dental management</json:string><json:string>ocular</json:string><json:string>gingival maturation</json:string><json:string>community services</json:string><json:string>ocular features</json:string><json:string>craniofacial features</json:string><json:string>dental department</json:string><json:string>family history</json:string><json:string>neural crest cells</json:string><json:string>maxillary hypodontia</json:string><json:string>dental literature</json:string><json:string>axenfeld syndrome</json:string><json:string>mandibular teeth</json:string><json:string>first molar</json:string><json:string>partial denture</json:string><json:string>little information</json:string><json:string>anterior chamber</json:string><json:string>somatic anomalies</json:string><json:string>restorative care</json:string><json:string>dietary advice</json:string><json:string>bone density</json:string><json:string>periumbilical skin</json:string><json:string>orthodontic treatment</json:string><json:string>periodontal disease</json:string><json:string>wide variety</json:string></teeft></keywords><author><json:item><name>Jennie M. Waldron BDS, NUI</name><affiliations><json:string>Vocational Trainee, Dental Department, Community Services, Mayo, Ireland</json:string></affiliations></json:item><json:item><name>Clare McNamara BDentSc, MSc, M Orth, FDS RCS (Eng)</name><affiliations><json:string>Senior Registrar, Department of Orthodontics, Gloucester Royal Hospital, Gloucestershire, UK</json:string></affiliations></json:item><json:item><name>Antonia R. Hewson BDS, NUI, M Med Sc</name><affiliations><json:string>Principal Dental Surgeon, Dental Department, Community Services, Mayo, Ireland</json:string></affiliations></json:item><json:item><name>C.M. McNamara BDS, D Orth, FDS RCS (Eng.)</name><affiliations><json:string>Consultant Orthodontist, HSE, Ireland.</json:string><json:string>E-mail: triona.mcnamara@gmail.com</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Axenfeld–Rieger syndrome</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>osteopenia</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>hypodontia</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>midface hypoplasia</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>ocular abnormalities</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>umbilical dysmorphology</value></json:item></subject><articleId><json:string>SCD153</json:string></articleId><arkIstex>ark:/67375/WNG-J9GXTDHT-X</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>Axenfeld–Rieger syndrome (ARS) is a rare, autosomal dominant condition characterized by ocular, craniofacial, dental, and periumbilical abnormalities. Relatively little information exists on this syndrome within the dental literature despite the fact that midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome. This is a case report of a 7‐year‐old Caucasian female with ARS who presented with significant ocular and dental anomalies. She was also found to have osteopenia. 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key="IE"></country></address></affiliation></author><author xml:id="author-0001"><persName><forename type="first">Clare</forename><surname>McNamara</surname><roleName type="degree">BDentSc, MSc, M Orth, FDS RCS (Eng)</roleName></persName><affiliation>Senior Registrar, Department of Orthodontics, Gloucester Royal Hospital, Gloucestershire, UK<address><country key="GB"></country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">Antonia R.</forename><surname>Hewson</surname><roleName type="degree">BDS, NUI, M Med Sc</roleName></persName><affiliation>Principal Dental Surgeon, Dental Department, Community Services, Mayo, Ireland<address><country key="IE"></country></address></affiliation></author><author xml:id="author-0003" role="corresp"><persName><forename type="first">C.M.</forename><surname>McNamara</surname><roleName type="degree">BDS, D Orth, FDS RCS (Eng.)</roleName></persName><affiliation>Consultant Orthodontist, HSE, Ireland.<address><country key="IE"></country></address></affiliation><affiliation>Corresponding author e‐mail: triona.mcnamara@gmail.com</affiliation></author><idno type="istex">19B54ABF9FCB8E102A14D8121D5A5598C0285A67</idno><idno type="ark">ark:/67375/WNG-J9GXTDHT-X</idno><idno type="DOI">10.1111/j.1754-4505.2010.00153.x</idno><idno type="unit">SCD153</idno><idno type="toTypesetVersion">file:SCD.SCD153.pdf</idno></analytic><monogr><title level="j" type="main">Special Care in Dentistry</title><title level="j" type="alt">SPECIAL CARE IN DENTISTRY</title><idno type="pISSN">0275-1879</idno><idno type="eISSN">1754-4505</idno><idno type="book-DOI">10.1111/(ISSN)1754-4505</idno><idno type="book-part-DOI">10.1111/scd.2010.30.issue-5</idno><idno type="product">SCD</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">30</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="218">218</biblScope><biblScope unit="page" 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Relatively little information exists on this syndrome within the dental literature despite the fact that midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome.</p><p>This is a case report of a 7‐year‐old Caucasian female with ARS who presented with significant ocular and dental anomalies. She was also found to have osteopenia. Her dental condition is described, her immediate treatment is shown, and her long‐term treatment needs are discussed.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1">Axenfeld–Rieger syndrome</term><term xml:id="k2">osteopenia</term><term xml:id="k3">hypodontia</term><term xml:id="k4">midface hypoplasia</term><term xml:id="k5">ocular abnormalities</term><term xml:id="k6">umbilical dysmorphology</term></keywords><keywords rend="tocHeading1"><term>ARTICLE</term></keywords></textClass><langUsage><language ident="en"></language></langUsage></profileDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/19B54ABF9FCB8E102A14D8121D5A5598C0285A67/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Publishing Inc</publisherName><publisherLoc>Malden, USA</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1754-4505</doi><issn type="print">0275-1879</issn><issn type="electronic">1754-4505</issn><idGroup><id type="product" value="SCD"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="SPECIAL CARE IN DENTISTRY">Special Care in Dentistry</title></titleGroup></publicationMeta><publicationMeta level="part" position="09105"><doi origin="wiley">10.1111/scd.2010.30.issue-5</doi><numberingGroup><numbering type="journalVolume" number="30">30</numbering><numbering type="journalIssue" number="5">5</numbering></numberingGroup><coverDate startDate="2010-09">September/October 2010</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="6" status="forIssue"><doi origin="wiley">10.1111/j.1754-4505.2010.00153.x</doi><idGroup><id type="unit" value="SCD153"></id></idGroup><countGroup><count type="pageTotal" number="5"></count></countGroup><titleGroup><title type="tocHeading1">ARTICLE</title></titleGroup><copyright>©2010 Special Care Dentistry Association and Wiley Periodicals, Inc.</copyright><eventGroup><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.18.1 mode:FullText" date="2010-09-10"></event><event type="publishedOnlineEarlyUnpaginated" date="2010-08-17"></event><event type="firstOnline" date="2010-08-17"></event><event type="publishedOnlineFinalForm" date="2010-09-10"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-08"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-11-03"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="218">218</numbering><numbering type="pageLast" number="222">222</numbering></numberingGroup><correspondenceTo>
Corresponding author e‐mail: <email>triona.mcnamara@gmail.com</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:SCD.SCD153.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="7"></count><count type="tableTotal" number="0"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="18"></count><count type="linksCrossRef" number="70"></count></countGroup><titleGroup><title type="main">ARTICLE: Axenfeld–Rieger Syndrome (ARS): A review and case report</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>Jennie M.</givenNames><familyName>Waldron</familyName><degrees>BDS, NUI</degrees></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a2"><personName><givenNames>Clare</givenNames><familyName>McNamara</familyName><degrees>BDentSc, MSc, M Orth, FDS RCS (Eng)</degrees></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a3"><personName><givenNames>Antonia R.</givenNames><familyName>Hewson</familyName><degrees>BDS, NUI, M Med Sc</degrees></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a4" corresponding="yes"><personName><givenNames>C.M.</givenNames><familyName>McNamara</familyName><degrees>BDS, D Orth, FDS RCS (Eng.)</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="IE"><unparsedAffiliation>Vocational Trainee, Dental Department, Community Services, Mayo, Ireland</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="GB"><unparsedAffiliation>Senior Registrar, Department of Orthodontics, Gloucester Royal Hospital, Gloucestershire, UK</unparsedAffiliation></affiliation><affiliation xml:id="a3" countryCode="IE"><unparsedAffiliation>Principal Dental Surgeon, Dental Department, Community Services, Mayo, Ireland</unparsedAffiliation></affiliation><affiliation xml:id="a4" countryCode="IE"><unparsedAffiliation>Consultant Orthodontist, HSE, Ireland.</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">Axenfeld–Rieger syndrome</keyword><keyword xml:id="k2">osteopenia</keyword><keyword xml:id="k3">hypodontia</keyword><keyword xml:id="k4">midface hypoplasia</keyword><keyword xml:id="k5">ocular abnormalities</keyword><keyword xml:id="k6">umbilical dysmorphology</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">ABSTRACT</title><p>Axenfeld–Rieger syndrome (ARS) is a rare, autosomal dominant condition characterized by ocular, craniofacial, dental, and periumbilical abnormalities. Relatively little information exists on this syndrome within the dental literature despite the fact that midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome.</p><p>This is a case report of a 7‐year‐old Caucasian female with ARS who presented with significant ocular and dental anomalies. She was also found to have osteopenia. Her dental condition is described, her immediate treatment is shown, and her long‐term treatment needs are discussed.</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="n-fnt-1" numbered="no"><p> <i>Spec Care Dentist 30(5):</i> 218‐222, 210</p></note></noteGroup></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>ARTICLE: Axenfeld–Rieger Syndrome (ARS): A review and case report</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>ARTICLE: Axenfeld–Rieger Syndrome (ARS): A review and case report</title></titleInfo><name type="personal"><namePart type="given">Jennie M.</namePart><namePart type="family">Waldron</namePart><namePart type="termsOfAddress">BDS, NUI</namePart><affiliation>Vocational Trainee, Dental Department, Community Services, Mayo, Ireland</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Clare</namePart><namePart type="family">McNamara</namePart><namePart type="termsOfAddress">BDentSc, MSc, M Orth, FDS RCS (Eng)</namePart><affiliation>Senior Registrar, Department of Orthodontics, Gloucester Royal Hospital, Gloucestershire, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Antonia R.</namePart><namePart type="family">Hewson</namePart><namePart type="termsOfAddress">BDS, NUI, M Med Sc</namePart><affiliation>Principal Dental Surgeon, Dental Department, Community Services, Mayo, Ireland</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C.M.</namePart><namePart type="family">McNamara</namePart><namePart type="termsOfAddress">BDS, D Orth, FDS RCS (Eng.)</namePart><affiliation>Consultant Orthodontist, HSE, Ireland.</affiliation><affiliation>E-mail: triona.mcnamara@gmail.com</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</genre><originInfo><publisher>Blackwell Publishing Inc</publisher><place><placeTerm type="text">Malden, USA</placeTerm></place><dateIssued encoding="w3cdtf">2010-09</dateIssued><copyrightDate encoding="w3cdtf">2010</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">7</extent><extent unit="tables">0</extent><extent unit="formulas">0</extent><extent unit="references">18</extent><extent unit="linksCrossRef">70</extent></physicalDescription><abstract lang="en">Axenfeld–Rieger syndrome (ARS) is a rare, autosomal dominant condition characterized by ocular, craniofacial, dental, and periumbilical abnormalities. Relatively little information exists on this syndrome within the dental literature despite the fact that midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome. This is a case report of a 7‐year‐old Caucasian female with ARS who presented with significant ocular and dental anomalies. She was also found to have osteopenia. Her dental condition is described, her immediate treatment is shown, and her long‐term treatment needs are discussed.</abstract><subject lang="en"><genre>keywords</genre><topic>Axenfeld–Rieger syndrome</topic><topic>osteopenia</topic><topic>hypodontia</topic><topic>midface hypoplasia</topic><topic>ocular abnormalities</topic><topic>umbilical dysmorphology</topic></subject><relatedItem type="host"><titleInfo><title>Special Care in Dentistry</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><identifier type="ISSN">0275-1879</identifier><identifier type="eISSN">1754-4505</identifier><identifier type="DOI">10.1111/(ISSN)1754-4505</identifier><identifier type="PublisherID">SCD</identifier><part><date>2010</date><detail type="volume"><caption>vol.</caption><number>30</number></detail><detail type="issue"><caption>no.</caption><number>5</number></detail><extent unit="pages"><start>218</start><end>222</end><total>5</total></extent></part></relatedItem><identifier type="istex">19B54ABF9FCB8E102A14D8121D5A5598C0285A67</identifier><identifier type="ark">ark:/67375/WNG-J9GXTDHT-X</identifier><identifier type="DOI">10.1111/j.1754-4505.2010.00153.x</identifier><identifier type="ArticleID">SCD153</identifier><accessCondition type="use and reproduction" contentType="copyright">©2010 Special Care Dentistry Association and Wiley Periodicals, Inc.</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource><recordOrigin>Blackwell Publishing Inc</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/19B54ABF9FCB8E102A14D8121D5A5598C0285A67/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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