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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Papillon–Lefevre syndrome: Reporting consanguinity as a risk factor</title>
<author><name sortKey="Shah, Aasim Farooq" sort="Shah, Aasim Farooq" uniqKey="Shah A" first="Aasim Farooq" last="Shah">Aasim Farooq Shah</name>
<affiliation><nlm:aff id="af005">Department of Public Health Dentistry, Kothiwal Dental College & Research Centre, Kanth Road, Moradabad 244001, Uttar Pradesh, India</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Tangade, Pradeep" sort="Tangade, Pradeep" uniqKey="Tangade P" first="Pradeep" last="Tangade">Pradeep Tangade</name>
<affiliation><nlm:aff id="af005">Department of Public Health Dentistry, Kothiwal Dental College & Research Centre, Kanth Road, Moradabad 244001, Uttar Pradesh, India</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Agarwal, Swatantra" sort="Agarwal, Swatantra" uniqKey="Agarwal S" first="Swatantra" last="Agarwal">Swatantra Agarwal</name>
<affiliation><nlm:aff id="af010">Department of Prosthodontics, Kothiwal Dental College & Research Centre, Kanth Road, Moradabad 244001, Uttar Pradesh, India</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">25057233</idno>
<idno type="pmc">4095039</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4095039</idno>
<idno type="RBID">PMC:4095039</idno>
<idno type="doi">10.1016/j.sdentj.2014.02.004</idno>
<date when="2014">2014</date>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Papillon–Lefevre syndrome: Reporting consanguinity as a risk factor</title>
<author><name sortKey="Shah, Aasim Farooq" sort="Shah, Aasim Farooq" uniqKey="Shah A" first="Aasim Farooq" last="Shah">Aasim Farooq Shah</name>
<affiliation><nlm:aff id="af005">Department of Public Health Dentistry, Kothiwal Dental College & Research Centre, Kanth Road, Moradabad 244001, Uttar Pradesh, India</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Tangade, Pradeep" sort="Tangade, Pradeep" uniqKey="Tangade P" first="Pradeep" last="Tangade">Pradeep Tangade</name>
<affiliation><nlm:aff id="af005">Department of Public Health Dentistry, Kothiwal Dental College & Research Centre, Kanth Road, Moradabad 244001, Uttar Pradesh, India</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Agarwal, Swatantra" sort="Agarwal, Swatantra" uniqKey="Agarwal S" first="Swatantra" last="Agarwal">Swatantra Agarwal</name>
<affiliation><nlm:aff id="af010">Department of Prosthodontics, Kothiwal Dental College & Research Centre, Kanth Road, Moradabad 244001, Uttar Pradesh, India</nlm:aff>
</affiliation>
</author>
</analytic>
<series><title level="j">The Saudi Dental Journal</title>
<idno type="ISSN">1013-9052</idno>
<idno type="eISSN">1658-3558</idno>
<imprint><date when="2014">2014</date>
</imprint>
</series>
</biblStruct>
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<front><div type="abstract" xml:lang="en"><p>Papillon–Lefevre syndrome (PLS) is an autosomal recessive genetic disorder characterized by palmoplantar hyperkeratosis associated with severe early-onset periodontitis and premature loss of primary and permanent teeth. This report describes two cases of PLS in 28-year-old female and 16-year-old male siblings with consanguineously married parents. The patients presented to the Department of Public Health Dentistry of a dental education and research institute in India with thickening, flaking, and scaling of the skin on the palms and soles of the feet. On oral examination, the female patient presented completely resorbed maxillary and mandibular alveolar ridges with retention of only the third molars. The male patient retained only teeth 18, 13, 28, 38, and 45. Based on complete histories and clinical examination findings, a final diagnosis of PLS was made and treatment was initiated using an interdisciplinary dental approach in both cases.</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">Saudi Dent J</journal-id>
<journal-id journal-id-type="iso-abbrev">Saudi Dent J</journal-id>
<journal-title-group><journal-title>The Saudi Dental Journal</journal-title>
</journal-title-group>
<issn pub-type="ppub">1013-9052</issn>
<issn pub-type="epub">1658-3558</issn>
<publisher><publisher-name>Elsevier</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">25057233</article-id>
<article-id pub-id-type="pmc">4095039</article-id>
<article-id pub-id-type="publisher-id">S1013-9052(14)00031-5</article-id>
<article-id pub-id-type="doi">10.1016/j.sdentj.2014.02.004</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group><article-title>Papillon–Lefevre syndrome: Reporting consanguinity as a risk factor</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Shah</surname>
<given-names>Aasim Farooq</given-names>
</name>
<email>dr_aasimshah@yahoo.com</email>
<xref rid="af005" ref-type="aff">a</xref>
<xref rid="cor1" ref-type="corresp">⁎</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Tangade</surname>
<given-names>Pradeep</given-names>
</name>
<email>ptangade@rediffmail.com</email>
<xref rid="af005" ref-type="aff">a</xref>
<xref rid="fn1" ref-type="fn">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Agarwal</surname>
<given-names>Swatantra</given-names>
</name>
<email>drswatantra@yahoo.co.in</email>
<xref rid="af010" ref-type="aff">b</xref>
<xref rid="fn2" ref-type="fn">2</xref>
</contrib>
</contrib-group>
<aff id="af005"><label>a</label>
Department of Public Health Dentistry, Kothiwal Dental College & Research Centre, Kanth Road, Moradabad 244001, Uttar Pradesh, India</aff>
<aff id="af010"><label>b</label>
Department of Prosthodontics, Kothiwal Dental College & Research Centre, Kanth Road, Moradabad 244001, Uttar Pradesh, India</aff>
<author-notes><corresp id="cor1"><label>⁎</label>
Corresponding author. Mobile: +91 9456910498. <email>dr_aasimshah@yahoo.com</email>
</corresp>
<fn id="fn1"><label>1</label>
<p>Mobile: +91 9997466339; fax: +91 0591 2452996.</p>
</fn>
<fn id="fn2"><label>2</label>
<p>Mobile: +91 9837043736.</p>
</fn>
</author-notes>
<pub-date pub-type="pmc-release"><day>19</day>
<month>4</month>
<year>2014</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="epub"><day>19</day>
<month>4</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="ppub"><month>7</month>
<year>2014</year>
</pub-date>
<volume>26</volume>
<issue>3</issue>
<fpage>126</fpage>
<lpage>131</lpage>
<history><date date-type="received"><day>17</day>
<month>10</month>
<year>2013</year>
</date>
<date date-type="rev-recd"><day>31</day>
<month>12</month>
<year>2013</year>
</date>
<date date-type="accepted"><day>11</day>
<month>2</month>
<year>2014</year>
</date>
</history>
<permissions><copyright-statement>© 2014 King Saud University. Production and Hosting by Elsevier B.V. All rights reserved.</copyright-statement>
<copyright-year>2014</copyright-year>
<copyright-holder>King Saud University</copyright-holder>
</permissions>
<abstract><p>Papillon–Lefevre syndrome (PLS) is an autosomal recessive genetic disorder characterized by palmoplantar hyperkeratosis associated with severe early-onset periodontitis and premature loss of primary and permanent teeth. This report describes two cases of PLS in 28-year-old female and 16-year-old male siblings with consanguineously married parents. The patients presented to the Department of Public Health Dentistry of a dental education and research institute in India with thickening, flaking, and scaling of the skin on the palms and soles of the feet. On oral examination, the female patient presented completely resorbed maxillary and mandibular alveolar ridges with retention of only the third molars. The male patient retained only teeth 18, 13, 28, 38, and 45. Based on complete histories and clinical examination findings, a final diagnosis of PLS was made and treatment was initiated using an interdisciplinary dental approach in both cases.</p>
</abstract>
<kwd-group><title>Keywords</title>
<kwd>Papillon–Lefevre syndrome</kwd>
<kwd>Consanguinity</kwd>
<kwd>Periodontitis</kwd>
<kwd>Premature tooth loss</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>
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