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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Prosthodontic management of patients with Christ–Siemens–Touraine syndrome</title><author><name sortKey="Shigli, Anand" sort="Shigli, Anand" uniqKey="Shigli A" first="Anand" last="Shigli">Anand Shigli</name></author><author><name sortKey="Airen Sarkar, Priyanka" sort="Airen Sarkar, Priyanka" uniqKey="Airen Sarkar P" first="Priyanka" last="Airen Sarkar">Priyanka Airen Sarkar</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">22744257</idno><idno type="pmc">3448356</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448356</idno><idno type="RBID">PMC:3448356</idno><idno type="doi">10.1136/bcr.11.2011.5226</idno><date when="2012">2012</date><idno type="wicri:Area/Pmc/Corpus">000087</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000087</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Prosthodontic management of patients with Christ–Siemens–Touraine syndrome</title><author><name sortKey="Shigli, Anand" sort="Shigli, Anand" uniqKey="Shigli A" first="Anand" last="Shigli">Anand Shigli</name></author><author><name sortKey="Airen Sarkar, Priyanka" sort="Airen Sarkar, Priyanka" uniqKey="Airen Sarkar P" first="Priyanka" last="Airen Sarkar">Priyanka Airen Sarkar</name></author></analytic><series><title level="j">BMJ Case Reports</title><idno type="eISSN">1757-790X</idno><imprint><date when="2012">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Christ–Siemens–Touraine syndrome also known as anhidrotic ectodermal dysplasia. Ectodermal dysplasia is a hereditary disorder characterised by developmental dystrophies of ectodermal derivatives. It is characterised by triad of signs comprising sparse hair, abnormal or missing teeth and inability to sweat. Anodontia or hypodontia is the most striking dental manifestation. In severe hypodontia, there is lack of alveolar development with consequent protrusion and eversion of the lips. The case of three children with anhidrotic ectodermal dysplasia with partial anodontia is presented. Dental, oral and physical features were taken into consideration in diagnosis and different treatment modalities for this patient. Clinical management consisted of removable partial prosthesis in maxillary arch and complete denture prosthesis in mandibular arch. The main aim of the treatment was to improve psychological development and to promote better functioning of the stomatognathic system.</p></div></front></TEI><pmc article-type="case-report"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">BMJ Case Rep</journal-id><journal-id journal-id-type="iso-abbrev">BMJ Case Rep</journal-id><journal-id journal-id-type="hwp">casereports</journal-id><journal-id journal-id-type="publisher-id">bmjcasereports</journal-id><journal-title-group><journal-title>BMJ Case Reports</journal-title></journal-title-group><issn pub-type="epub">1757-790X</issn><publisher><publisher-name>BMJ Publishing Group</publisher-name><publisher-loc>BMA House, Tavistock Square, London, WC1H 9JR</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">22744257</article-id><article-id pub-id-type="pmc">3448356</article-id><article-id pub-id-type="publisher-id">bcr.11.2011.5226</article-id><article-id pub-id-type="doi">10.1136/bcr.11.2011.5226</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group><subj-group subj-group-type="hwp-journal-coll"><subject>1527</subject><subject>55</subject><subject>1304</subject><subject>1319</subject><subject>1560</subject></subj-group><subj-group subj-group-type="case-report-type"><subject>Unusual Presentation of More Common Disease/Injury</subject></subj-group><subj-group subj-group-type="search-fields"><subject>Male</subject><subject>6–12 Years</subject><subject>Indian Sub-Continent</subject><subject>Asia</subject></subj-group><subj-group subj-group-type="search-fields"><subject>Male</subject><subject>6–12 Years</subject><subject>Indian Sub-Continent</subject><subject>Asia</subject></subj-group><series-title>Unusual presentation of more common disease/injury</series-title></article-categories><title-group><article-title>Prosthodontic management of patients with Christ–Siemens–Touraine syndrome</article-title><alt-title alt-title-type="running-head">Unusual presentation of more common disease/injury</alt-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Shigli</surname><given-names>Anand</given-names></name></contrib><contrib contrib-type="author"><name><surname>Airen Sarkar</surname><given-names>Priyanka</given-names></name></contrib></contrib-group><aff>Pediatric Dentistry Department, Modern Dental College and Research Centre, Indore, Madhya Pradesh, India</aff><author-notes><corresp><label>Correspondence to</label> Dr Priyanka Airen Sarkar, <email>priyankairen@gmail.com</email></corresp></author-notes><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>27</day><month>7</month><year>2012</year></pub-date><volume>2012</volume><elocation-id>bcr1120115226</elocation-id><permissions><copyright-statement>2012 BMJ Publishing Group Ltd</copyright-statement><copyright-year>2012</copyright-year></permissions><self-uri xlink:title="pdf" xlink:type="simple" xlink:href="bcr.11.2011.5226.pdf"></self-uri><abstract><p>Christ–Siemens–Touraine syndrome also known as anhidrotic ectodermal dysplasia. Ectodermal dysplasia is a hereditary disorder characterised by developmental dystrophies of ectodermal derivatives. It is characterised by triad of signs comprising sparse hair, abnormal or missing teeth and inability to sweat. Anodontia or hypodontia is the most striking dental manifestation. In severe hypodontia, there is lack of alveolar development with consequent protrusion and eversion of the lips. The case of three children with anhidrotic ectodermal dysplasia with partial anodontia is presented. Dental, oral and physical features were taken into consideration in diagnosis and different treatment modalities for this patient. Clinical management consisted of removable partial prosthesis in maxillary arch and complete denture prosthesis in mandibular arch. The main aim of the treatment was to improve psychological development and to promote better functioning of the stomatognathic system.</p></abstract></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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