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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Witkop's syndrome: A case report</title><author><name sortKey="Arora, Varuni" sort="Arora, Varuni" uniqKey="Arora V" first="Varuni" last="Arora">Varuni Arora</name><affiliation><nlm:aff id="aff0005">Senior Resident, Department of Prosthodontics, Crowns & Bridges, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</nlm:aff></affiliation></author><author><name sortKey="Agrawal, Kaushal Kishor" sort="Agrawal, Kaushal Kishor" uniqKey="Agrawal K" first="Kaushal Kishor" last="Agrawal">Kaushal Kishor Agrawal</name><affiliation><nlm:aff id="aff0010">Assistant Professor, Department of Prosthodontics, Crowns & Bridges, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</nlm:aff></affiliation></author><author><name sortKey="Mishra, Apurva" sort="Mishra, Apurva" uniqKey="Mishra A" first="Apurva" last="Mishra">Apurva Mishra</name><affiliation><nlm:aff id="aff0015">Senior Resident, Department of Paediatric and Preventive Dentistry, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</nlm:aff></affiliation></author><author><name sortKey="Chandra, Anil" sort="Chandra, Anil" uniqKey="Chandra A" first="Anil" last="Chandra">Anil Chandra</name><affiliation><nlm:aff id="aff0020">Professor, Department of Endodontics and Conservative Dentistry Crowns & Bridges, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">26937375</idno><idno type="pmc">4756068</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756068</idno><idno type="RBID">PMC:4756068</idno><idno type="doi">10.1016/j.jobcr.2015.07.003</idno><date when="2015">2015</date><idno type="wicri:Area/Pmc/Corpus">001935</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001935</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Witkop's syndrome: A case report</title><author><name sortKey="Arora, Varuni" sort="Arora, Varuni" uniqKey="Arora V" first="Varuni" last="Arora">Varuni Arora</name><affiliation><nlm:aff id="aff0005">Senior Resident, Department of Prosthodontics, Crowns & Bridges, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</nlm:aff></affiliation></author><author><name sortKey="Agrawal, Kaushal Kishor" sort="Agrawal, Kaushal Kishor" uniqKey="Agrawal K" first="Kaushal Kishor" last="Agrawal">Kaushal Kishor Agrawal</name><affiliation><nlm:aff id="aff0010">Assistant Professor, Department of Prosthodontics, Crowns & Bridges, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</nlm:aff></affiliation></author><author><name sortKey="Mishra, Apurva" sort="Mishra, Apurva" uniqKey="Mishra A" first="Apurva" last="Mishra">Apurva Mishra</name><affiliation><nlm:aff id="aff0015">Senior Resident, Department of Paediatric and Preventive Dentistry, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</nlm:aff></affiliation></author><author><name sortKey="Chandra, Anil" sort="Chandra, Anil" uniqKey="Chandra A" first="Anil" last="Chandra">Anil Chandra</name><affiliation><nlm:aff id="aff0020">Professor, Department of Endodontics and Conservative Dentistry Crowns & Bridges, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</nlm:aff></affiliation></author></analytic><series><title level="j">Journal of Oral Biology and Craniofacial Research</title><idno type="ISSN">2212-4268</idno><idno type="eISSN">2212-4276</idno><imprint><date when="2015">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Witkop's syndrome is a rare autosomal dominant disorder characterized by tooth and nail abnormalities. It is a variant of ectodermal dysplasia, which is thought to occur in approximately 1 in 100,000 live births. Thus, such a low occurrence and paucity of clearly delineating features make its identification in general population a real challenge. This case report aims to add to the existing literature a commonsense approach of identifying the uncommon thing.</p></div></front></TEI><pmc article-type="brief-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">J Oral Biol Craniofac Res</journal-id><journal-id journal-id-type="iso-abbrev">J Oral Biol Craniofac Res</journal-id><journal-title-group><journal-title>Journal of Oral Biology and Craniofacial Research</journal-title></journal-title-group><issn pub-type="ppub">2212-4268</issn><issn pub-type="epub">2212-4276</issn><publisher><publisher-name>Elsevier</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">26937375</article-id><article-id pub-id-type="pmc">4756068</article-id><article-id pub-id-type="publisher-id">S2212-4268(15)00075-5</article-id><article-id pub-id-type="doi">10.1016/j.jobcr.2015.07.003</article-id><article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject></subj-group></article-categories><title-group><article-title>Witkop's syndrome: A case report</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Arora</surname><given-names>Varuni</given-names></name><email>varu.varuni@gmail.com</email><xref rid="aff0005" ref-type="aff">a</xref><xref rid="cor0005" ref-type="corresp">⁎</xref></contrib><contrib contrib-type="author"><name><surname>Agrawal</surname><given-names>Kaushal Kishor</given-names></name><xref rid="aff0010" ref-type="aff">b</xref></contrib><contrib contrib-type="author"><name><surname>Mishra</surname><given-names>Apurva</given-names></name><xref rid="aff0015" ref-type="aff">c</xref></contrib><contrib contrib-type="author"><name><surname>Chandra</surname><given-names>Anil</given-names></name><xref rid="aff0020" ref-type="aff">d</xref></contrib></contrib-group><aff id="aff0005"><label>a</label>Senior Resident, Department of Prosthodontics, Crowns & Bridges, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</aff><aff id="aff0010"><label>b</label>Assistant Professor, Department of Prosthodontics, Crowns & Bridges, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</aff><aff id="aff0015"><label>c</label>Senior Resident, Department of Paediatric and Preventive Dentistry, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</aff><aff id="aff0020"><label>d</label>Professor, Department of Endodontics and Conservative Dentistry Crowns & Bridges, Faculty of Dental Sciences, King George's Medical University UP, Lucknow, Uttar Pradesh, India</aff><author-notes><corresp id="cor0005"><label>⁎</label><italic>Corresponding author</italic>. <email>varu.varuni@gmail.com</email></corresp></author-notes><pub-date pub-type="pmc-release"><day>19</day><month>12</month><year>2015</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><season>Jan-Apr</season><year>2016</year></pub-date><pub-date pub-type="epub"><day>19</day><month>12</month><year>2015</year></pub-date><volume>6</volume><issue>1</issue><fpage>79</fpage><lpage>81</lpage><history><date date-type="received"><day>29</day><month>6</month><year>2015</year></date><date date-type="accepted"><day>8</day><month>7</month><year>2015</year></date></history><permissions><copyright-statement>© 2015 Craniofacial Research Foundation. Published by Elsevier B.V. All rights reserved.</copyright-statement><copyright-year>2015</copyright-year><copyright-holder>Craniofacial Research Foundation</copyright-holder></permissions><abstract><p>Witkop's syndrome is a rare autosomal dominant disorder characterized by tooth and nail abnormalities. It is a variant of ectodermal dysplasia, which is thought to occur in approximately 1 in 100,000 live births. Thus, such a low occurrence and paucity of clearly delineating features make its identification in general population a real challenge. This case report aims to add to the existing literature a commonsense approach of identifying the uncommon thing.</p></abstract><kwd-group><title>Keywords</title><kwd>Dysgenesis of nails</kwd><kwd>Hypodontia</kwd><kwd>MSX-1</kwd><kwd>Oligodontia</kwd><kwd>Tooth and nail syndrome</kwd></kwd-group></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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