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Ehlers Danlos Syndrome – A Case Report

Identifieur interne : 000343 ( Pmc/Checkpoint ); précédent : 000342; suivant : 000344

Ehlers Danlos Syndrome – A Case Report

Auteurs : Pragati Kaurani ; Nikhil Marwah ; Mayank Kaurani ; Narendra Padiyar

Source :

RBID : PMC:4003659

Abstract

Ehlers Danlos syndrome (EDS) is a hereditary collagen disorder which primarily manifests in the skin and joints. Clinically, it is characterized by hyperelasticity of skin and joint hypermobility. This article has described a rare condition seen in a 10-year-old boy who was diagnosed with EDS, based on the clinical, radiographic and histological findings.


Url:
DOI: 10.7860/JCDR/2014/4569.4178
PubMed: 24783151
PubMed Central: 4003659


Affiliations:


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PMC:4003659

Le document en format XML

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<nlm:aff id="aff1">Reader, Department of Prosthodontics,
<institution> Mahatma Gandhi Dental College and Hospital</institution>
,
<addr-line>Jaipur, India</addr-line>
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<name sortKey="Marwah, Nikhil" sort="Marwah, Nikhil" uniqKey="Marwah N" first="Nikhil" last="Marwah">Nikhil Marwah</name>
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<nlm:aff id="aff2">Professor, Department of Paedriatic and Preventive Dentistry,
<institution> Mahatma Gandhi Dental College and Hospital</institution>
,
<addr-line>Jaipur, India</addr-line>
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<name sortKey="Kaurani, Mayank" sort="Kaurani, Mayank" uniqKey="Kaurani M" first="Mayank" last="Kaurani">Mayank Kaurani</name>
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<nlm:aff id="aff3">Reader, Department of Endontics ,
<institution> Mahatma Gandhi Dental College and Hospital</institution>
,
<addr-line>Jaipur, India</addr-line>
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<name sortKey="Padiyar, Narendra" sort="Padiyar, Narendra" uniqKey="Padiyar N" first="Narendra" last="Padiyar">Narendra Padiyar</name>
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<nlm:aff id="aff4">Professor and HOD,
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,
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<nlm:aff id="aff3">Reader, Department of Endontics ,
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,
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.</nlm:aff>
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<name sortKey="Padiyar, Narendra" sort="Padiyar, Narendra" uniqKey="Padiyar N" first="Narendra" last="Padiyar">Narendra Padiyar</name>
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<nlm:aff id="aff4">Professor and HOD,
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,
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<title level="j">Journal of Clinical and Diagnostic Research : JCDR</title>
<idno type="ISSN">2249-782X</idno>
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<div type="abstract" xml:lang="en">
<p>Ehlers Danlos syndrome (EDS) is a hereditary collagen disorder which primarily manifests in the skin and joints. Clinically, it is characterized by hyperelasticity of skin and joint hypermobility. This article has described a rare condition seen in a 10-year-old boy who was diagnosed with EDS, based on the clinical, radiographic and histological findings.</p>
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<journal-id journal-id-type="nlm-ta">J Clin Diagn Res</journal-id>
<journal-id journal-id-type="iso-abbrev">J Clin Diagn Res</journal-id>
<journal-id journal-id-type="hwp">Journal of Clinical and Diagnostic Research</journal-id>
<journal-id journal-id-type="publisher-id">JCDR</journal-id>
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<issn pub-type="epub">0973-709X</issn>
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<publisher-loc>Delhi, India</publisher-loc>
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<subject>Dentistry</subject>
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<subject>Dental Case Report</subject>
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</subj-group>
</article-categories>
<title-group>
<article-title>Ehlers Danlos Syndrome – A Case Report</article-title>
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<name>
<surname>Kaurani</surname>
<given-names>Pragati</given-names>
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<surname>Marwah</surname>
<given-names>Nikhil</given-names>
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<surname>Kaurani</surname>
<given-names>Mayank</given-names>
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Reader, Department of Prosthodontics,
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Professor, Department of Paedriatic and Preventive Dentistry,
<institution> Mahatma Gandhi Dental College and Hospital</institution>
,
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Reader, Department of Endontics ,
<institution> Mahatma Gandhi Dental College and Hospital</institution>
,
<addr-line>Jaipur, India</addr-line>
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<label>4</label>
Professor and HOD,
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<author-notes>
<corresp id="cor1">NAME, ADDRESS, E-MAIL ID OF THE CORRESPONDING AUTHOR: Dr. Pragati Kaurani, C-31, Pratap Marg, Tilak Nagar, Jaipur-203004, India. Phone: 9829663314, E-mail:
<email>smile.pragati@gmail.com</email>
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<pub-date pub-type="ppub">
<month>3</month>
<year>2014</year>
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<pub-date pub-type="epub">
<day>15</day>
<month>3</month>
<year>2014</year>
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<volume>8</volume>
<issue>3</issue>
<fpage>256</fpage>
<lpage>258</lpage>
<history>
<date date-type="received">
<day>09</day>
<month>8</month>
<year>2013</year>
</date>
<date date-type="rev-request">
<day>20</day>
<month>12</month>
<year>2013</year>
</date>
<date date-type="accepted">
<day>14</day>
<month>1</month>
<year>2014</year>
</date>
</history>
<permissions>
<copyright-statement>© 2014 Journal of Clinical and Diagnostic Research</copyright-statement>
<copyright-year>2014</copyright-year>
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<abstract>
<p>Ehlers Danlos syndrome (EDS) is a hereditary collagen disorder which primarily manifests in the skin and joints. Clinically, it is characterized by hyperelasticity of skin and joint hypermobility. This article has described a rare condition seen in a 10-year-old boy who was diagnosed with EDS, based on the clinical, radiographic and histological findings.</p>
</abstract>
<kwd-group>
<kwd>Hereditary collagen disorders</kwd>
<kwd>Connective tissue disorder</kwd>
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