Clinical approach in familial hypophosphatemic rickets: report of three generations
Identifieur interne : 007E46 ( Istex/Corpus ); précédent : 007E45; suivant : 007E47Clinical approach in familial hypophosphatemic rickets: report of three generations
Auteurs : Eduardo Costa Studart Soares ; Fábio Wildson Gurgel Costa ; Thyciana Rodrigues Ribeiro ; Ana Paula Negreiros Nunes Alves ; Cristiane Sá Roriz FontelesSource :
- Special Care in Dentistry [ 0275-1879 ] ; 2013-11.
English descriptors
- KwdEn :
- Abscess, Adult patients, Arabic numerals, Black arrow, Bone loss, Cear, Clinical dentistry, Deciduous, Deciduous dentition, Deciduous teeth, Dental management, Dental treatment, Dentin, Dentistry, Dentition, Differential diagnosis, Dominant trait, Early diagnosis, Early loss, Endod, Familial hypophosphatemic rickets, Federal university, First evidences, Gingival, Histologic, Hypophosphatemic, Hypophosphatemic rickets, Initial presentation, Large pulp chambers, Many teeth, Molar, Multiple tooth loss, Numeral, Oral findings, Oral manifestations, Oral pathol, Oral surg, Panoramic, Panoramic radiography, Pediatric, Pediatric patients, Periodontal, Periodontal disease, Permanent dentitions, Phex gene, Present case report, Proband, Pulp horns, Radiographic, Radiol endod, Rickets, Roman numerals, Spontaneous gingival abscesses, White arrow, Xlhr.
- Teeft :
- Abscess, Adult patients, Arabic numerals, Black arrow, Bone loss, Cear, Clinical dentistry, Deciduous, Deciduous dentition, Deciduous teeth, Dental management, Dental treatment, Dentin, Dentistry, Dentition, Differential diagnosis, Dominant trait, Early diagnosis, Early loss, Endod, Familial hypophosphatemic rickets, Federal university, First evidences, Gingival, Histologic, Hypophosphatemic, Hypophosphatemic rickets, Initial presentation, Large pulp chambers, Many teeth, Molar, Multiple tooth loss, Numeral, Oral findings, Oral manifestations, Oral pathol, Oral surg, Panoramic, Panoramic radiography, Pediatric, Pediatric patients, Periodontal, Periodontal disease, Permanent dentitions, Phex gene, Present case report, Proband, Pulp horns, Radiographic, Radiol endod, Rickets, Roman numerals, Spontaneous gingival abscesses, White arrow, Xlhr.
Abstract
Familial hypophosphatemic rickets is a hereditary disease characterized by the involvement of several family members, transmitted in most cases as an X‐linked dominant trait. Oral manifestations can be the first evidences for an adequate and early diagnosis of X‐linked hypophosphatemic rickets (XLHR). The present report describes the main systemic manifestations, oral findings and dental management in three generations of an affected family. Oral exams, laboratorial and histologic evaluations, cone‐beam computed tomographies, panoramic and periapical radiographs were performed to properly institute the most adequate treatment strategy. The knowledge of clinical signs and symptoms of XLHR is essential for the correct diagnosis of this disease, and for the establishment of preventive and comprehensive dental care.
Url:
DOI: 10.1111/j.1754-4505.2012.00310.x
Links to Exploration step
ISTEX:FFB6EB12E25DD3B4E04618C254B9D11D9CB4DCE7Le document en format XML
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type="degree">DDS, MS, PhD</roleName></persName><affiliation><orgName>Full Professor, Department of Clinical Dentistry</orgName><orgName>Federal University of Ceará</orgName><address><settlement type="city">Fortaleza</settlement><country key="BR">Brazil</country></address></affiliation></author><author xml:id="author-0001"><persName><forename type="first">Fábio Wildson Gurgel</forename><surname>Costa</surname><roleName type="degree">DDS, MS</roleName></persName><affiliation><orgName>Assistant Professor, Department of Clinical Dentistry</orgName><orgName>Federal University of Ceará</orgName><address><region>Sobral</region><country key="BR">Brazil</country></address></affiliation></author><author xml:id="author-0002" role="corresp"><persName><forename type="first">Thyciana Rodrigues</forename><surname>Ribeiro</surname><roleName type="degree">DDS, MS</roleName></persName><affiliation><orgName>Ph.D. candidate, Postgraduate Program in Dentistry</orgName><orgName>Federal University of Ceará</orgName><address><settlement type="city">Fortaleza</settlement><country key="BR">Brazil</country></address></affiliation><affiliation>Corresponding author e‐mail: thyciana_odonto@yahoo.com</affiliation></author><author xml:id="author-0003"><persName><forename type="first">Ana Paula Negreiros Nunes</forename><surname>Alves</surname><roleName type="degree">DDS, MS, PhD</roleName></persName><affiliation><orgName>Associate Professor, Department of Clinical Dentistry</orgName><orgName>Federal University of Ceará</orgName><address><settlement type="city">Fortaleza</settlement><country key="BR">Brazil</country></address></affiliation></author><author xml:id="author-0004"><persName><forename type="first">Cristiane Sá Roriz</forename><surname>Fonteles</surname><roleName type="degree">DDS, MS, PhD</roleName></persName><affiliation><orgName>Associate Professor, Department of Clinical Dentistry</orgName><orgName>Federal University of Ceará</orgName><address><settlement 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Oral manifestations can be the first evidences for an adequate and early diagnosis of X‐linked hypophosphatemic rickets (XLHR). The present report describes the main systemic manifestations, oral findings and dental management in three generations of an affected family. Oral exams, laboratorial and histologic evaluations, cone‐beam computed tomographies, panoramic and periapical radiographs were performed to properly institute the most adequate treatment strategy. The knowledge of clinical signs and symptoms of XLHR is essential for the correct diagnosis of this disease, and for the establishment of preventive and comprehensive dental care.</p></abstract><textClass><keywords><term xml:id="scd310-kwd-0001">dental treatment</term><term xml:id="scd310-kwd-0002">oral medicine</term><term xml:id="scd310-kwd-0003">rickets</term></keywords><keywords rend="articleCategory"><term>Case History Report</term></keywords><keywords rend="tocHeading1"><term>Case History Reports</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/FFB6EB12E25DD3B4E04618C254B9D11D9CB4DCE7/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" 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position="90" type="caseStudy" status="forIssue"><doi origin="wiley">10.1111/j.1754-4505.2012.00310.x</doi><idGroup><id type="unit" value="SCD310"></id></idGroup><countGroup><count type="pageTotal" number="4"></count></countGroup><titleGroup><title type="articleCategory">Case History Report</title><title type="tocHeading1">Case History Reports</title></titleGroup><copyright ownership="publisher">©2012 Special Care Dentistry Association and Wiley Periodicals, Inc.</copyright><eventGroup><event type="xmlCreated" agent="Aptara" date="2012-11-09"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.2.6 mode:FullText" date="2013-10-25"></event><event type="publishedOnlineEarlyUnpaginated" date="2012-12-05"></event><event type="firstOnline" date="2012-12-05"></event><event type="publishedOnlineFinalForm" date="2013-10-25"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.6.4 mode:FullText" date="2015-10-03"></event></eventGroup><numberingGroup><numbering type="pageFirst">304</numbering><numbering type="pageLast">307</numbering></numberingGroup><correspondenceTo>Corresponding author e‐mail: <email>thyciana_odonto@yahoo.com</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:SCD.SCD310.pdf"></link></linkGroup></publicationMeta><contentMeta><titleGroup><title type="main">Clinical approach in familial hypophosphatemic rickets: report of three generations</title><title type="short">FAMILIAL HYPOPHOSPHATEMIC RICKETS</title><title type="shortAuthors">Soares et al.</title></titleGroup><creators><creator xml:id="scd310-cr-0001" creatorRole="author" affiliationRef="#scd310-aff-0001"><personName><givenNames>Eduardo Costa Studart</givenNames><familyName>Soares</familyName><degrees>DDS, MS, PhD</degrees></personName><jobTitle>Full Professor</jobTitle></creator><creator xml:id="scd310-cr-0002" creatorRole="author" affiliationRef="#scd310-aff-0002"><personName><givenNames>Fábio Wildson Gurgel</givenNames><familyName>Costa</familyName><degrees>DDS, MS</degrees></personName><jobTitle>Assistant Professor</jobTitle></creator><creator xml:id="scd310-cr-0003" creatorRole="author" affiliationRef="#scd310-aff-0003" corresponding="yes"><personName><givenNames>Thyciana Rodrigues</givenNames><familyName>Ribeiro</familyName><degrees>DDS, MS</degrees></personName><jobTitle>Ph.D. candidate</jobTitle></creator><creator xml:id="scd310-cr-0004" creatorRole="author" affiliationRef="#scd310-aff-0004"><personName><givenNames>Ana Paula Negreiros Nunes</givenNames><familyName>Alves</familyName><degrees>DDS, MS, PhD</degrees></personName><jobTitle>Associate Professor</jobTitle></creator><creator xml:id="scd310-cr-0005" creatorRole="author" affiliationRef="#scd310-aff-0004"><personName><givenNames>Cristiane Sá Roriz</givenNames><familyName>Fonteles</familyName><degrees>DDS, MS, PhD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="scd310-aff-0001" countryCode="BR"><orgDiv>Full Professor, Department of Clinical Dentistry</orgDiv><orgName>Federal University of Ceará</orgName><address><city>Fortaleza</city><country>Brazil</country></address></affiliation><affiliation xml:id="scd310-aff-0002" countryCode="BR"><orgDiv>Assistant Professor, Department of Clinical Dentistry</orgDiv><orgName>Federal University of Ceará</orgName><address><countryPart>Sobral</countryPart><country>Brazil</country></address></affiliation><affiliation xml:id="scd310-aff-0003" countryCode="BR"><orgDiv>Ph.D. candidate, Postgraduate Program in Dentistry</orgDiv><orgName>Federal University of Ceará</orgName><address><city>Fortaleza</city><country>Brazil</country></address></affiliation><affiliation xml:id="scd310-aff-0004" countryCode="BR"><orgDiv>Associate Professor, Department of Clinical Dentistry</orgDiv><orgName>Federal University of Ceará</orgName><address><city>Fortaleza</city><country>Brazil</country></address></affiliation></affiliationGroup><keywordGroup type="author"><keyword xml:id="scd310-kwd-0001">dental treatment</keyword><keyword xml:id="scd310-kwd-0002">oral medicine</keyword><keyword xml:id="scd310-kwd-0003">rickets</keyword></keywordGroup><abstractGroup><abstract type="main"><title type="main">ABSTRACT</title><p>Familial hypophosphatemic rickets is a hereditary disease characterized by the involvement of several family members, transmitted in most cases as an X‐linked dominant trait. Oral manifestations can be the first evidences for an adequate and early diagnosis of X‐linked hypophosphatemic rickets (XLHR). The present report describes the main systemic manifestations, oral findings and dental management in three generations of an affected family. Oral exams, laboratorial and histologic evaluations, cone‐beam computed tomographies, panoramic and periapical radiographs were performed to properly institute the most adequate treatment strategy. The knowledge of clinical signs and symptoms of XLHR is essential for the correct diagnosis of this disease, and for the establishment of preventive and comprehensive dental care.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Clinical approach in familial hypophosphatemic rickets: report of three generations</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>FAMILIAL HYPOPHOSPHATEMIC RICKETS</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Clinical approach in familial hypophosphatemic rickets: report of three generations</title></titleInfo><name type="personal"><namePart type="given">Eduardo Costa Studart</namePart><namePart type="family">Soares</namePart><namePart type="termsOfAddress">DDS, MS, PhD</namePart><affiliation>Full Professor, Department of Clinical Dentistry, Federal University of Ceará, Fortaleza, Brazil</affiliation><role><roleTerm type="text">author</roleTerm></role><description>Full Professor</description></name><name type="personal"><namePart type="given">Fábio Wildson Gurgel</namePart><namePart type="family">Costa</namePart><namePart type="termsOfAddress">DDS, MS</namePart><affiliation>Assistant Professor, Department of Clinical Dentistry, Federal University of Ceará, Sobral, Brazil</affiliation><role><roleTerm type="text">author</roleTerm></role><description>Assistant Professor</description></name><name type="personal"><namePart type="given">Thyciana Rodrigues</namePart><namePart type="family">Ribeiro</namePart><namePart type="termsOfAddress">DDS, MS</namePart><affiliation>Ph.D. candidate, Postgraduate Program in Dentistry, Federal University of Ceará, Fortaleza, Brazil</affiliation><affiliation>E-mail: thyciana_odonto@yahoo.com</affiliation><role><roleTerm type="text">author</roleTerm></role><description>Ph.D. candidate</description></name><name type="personal"><namePart type="given">Ana Paula Negreiros Nunes</namePart><namePart type="family">Alves</namePart><namePart type="termsOfAddress">DDS, MS, PhD</namePart><affiliation>Associate Professor, Department of Clinical Dentistry, Federal University of Ceará, Fortaleza, Brazil</affiliation><role><roleTerm type="text">author</roleTerm></role><description>Associate Professor</description></name><name type="personal"><namePart type="given">Cristiane Sá Roriz</namePart><namePart type="family">Fonteles</namePart><namePart type="termsOfAddress">DDS, MS, PhD</namePart><affiliation>Associate Professor, Department of Clinical Dentistry, Federal University of Ceará, Fortaleza, Brazil</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="case-report" displayLabel="caseStudy" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-29919SZJ-6">case-report</genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><dateIssued encoding="w3cdtf">2013-11</dateIssued><dateCreated encoding="w3cdtf">2012-11-09</dateCreated><copyrightDate encoding="w3cdtf">2013</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><abstract>Familial hypophosphatemic rickets is a hereditary disease characterized by the involvement of several family members, transmitted in most cases as an X‐linked dominant trait. Oral manifestations can be the first evidences for an adequate and early diagnosis of X‐linked hypophosphatemic rickets (XLHR). The present report describes the main systemic manifestations, oral findings and dental management in three generations of an affected family. Oral exams, laboratorial and histologic evaluations, cone‐beam computed tomographies, panoramic and periapical radiographs were performed to properly institute the most adequate treatment strategy. The knowledge of clinical signs and symptoms of XLHR is essential for the correct diagnosis of this disease, and for the establishment of preventive and comprehensive dental care.</abstract><subject><genre>keywords</genre><topic>dental treatment</topic><topic>oral medicine</topic><topic>rickets</topic></subject><relatedItem type="host"><titleInfo><title>Special Care in Dentistry</title></titleInfo><titleInfo type="abbreviated"><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><subject><genre>article-category</genre><topic>Case History Report</topic></subject><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>2013</date><detail type="volume"><caption>vol.</caption><number>33</number></detail><detail type="issue"><caption>no.</caption><number>6</number></detail><extent unit="pages"><start>304</start><end>307</end><total>4</total></extent></part></relatedItem><identifier type="istex">FFB6EB12E25DD3B4E04618C254B9D11D9CB4DCE7</identifier><identifier type="ark">ark:/67375/WNG-593QFTZT-2</identifier><identifier type="DOI">10.1111/j.1754-4505.2012.00310.x</identifier><identifier type="ArticleID">SCD310</identifier><accessCondition type="use and reproduction" contentType="copyright">© 2013 Special Care Dentistry Association and Wiley Periodicals, Inc.©2012 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></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/FFB6EB12E25DD3B4E04618C254B9D11D9CB4DCE7/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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