Prosthodontic Management of a Child with Ectodermal Dysplasia: A Case Report
Identifieur interne : 000920 ( Pmc/Corpus ); précédent : 000919; suivant : 000921Prosthodontic Management of a Child with Ectodermal Dysplasia: A Case Report
Auteurs : Akshay Bhargava ; Arun Sharma ; Sachet Popli ; Renu BhargavaSource :
- Journal of Indian Prosthodontic Society [ 0972-4052 ] ; 2010.
Abstract
Ectodermal dysplasia is a rare congenital disease that affects several ectodermal structures. Children with ectodermal dysplasia may have various manifestation of the disease that differ in severity and may or may not involve teeth, skin, hair, nails, sweat glands and sebaceous glands. The most common form of the ectodermal dysplasia syndrome is hypohidrotic ectodermal dysplasia and is usually inherited as an X-linked recessive trait. Female carriers may have a variable degree of clinical manifestations. This case report discusses the management of a 5-year-old girl with ectodermal dysplasia. Clinical management consisted of fabricating upper and lower dentures to help in psychosocial development and to restore the vertical dimension, esthetics and functioning of the stomatognathic system.
Url:
DOI: 10.1007/s13191-010-0026-9
PubMed: 21629459
PubMed Central: 3081263
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PMC:3081263Le document en format XML
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<author><name sortKey="Bhargava, Akshay" sort="Bhargava, Akshay" uniqKey="Bhargava A" first="Akshay" last="Bhargava">Akshay Bhargava</name>
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<affiliation><nlm:aff id="Aff3">Raahat Dental Clinic, 285, Type-A, Pkt.-1, Sec-23, Dwarka, New Delhi, 110075 India</nlm:aff>
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<author><name sortKey="Sharma, Arun" sort="Sharma, Arun" uniqKey="Sharma A" first="Arun" last="Sharma">Arun Sharma</name>
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<series><title level="j">Journal of Indian Prosthodontic Society</title>
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<front><div type="abstract" xml:lang="en"><p>Ectodermal dysplasia is a rare congenital disease that affects several ectodermal structures. Children with ectodermal dysplasia may have various manifestation of the disease that differ in severity and may or may not involve teeth, skin, hair, nails, sweat glands and sebaceous glands. The most common form of the ectodermal dysplasia syndrome is hypohidrotic ectodermal dysplasia and is usually inherited as an X-linked recessive trait. Female carriers may have a variable degree of clinical manifestations. This case report discusses the management of a 5-year-old girl with ectodermal dysplasia. Clinical management consisted of fabricating upper and lower dentures to help in psychosocial development and to restore the vertical dimension, esthetics and functioning of the stomatognathic system.</p>
</div>
</front>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">J Indian Prosthodont Soc</journal-id>
<journal-title-group><journal-title>Journal of Indian Prosthodontic Society</journal-title>
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<publisher><publisher-name>Springer-Verlag</publisher-name>
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<article-id pub-id-type="doi">10.1007/s13191-010-0026-9</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Clinical Report</subject>
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<title-group><article-title>Prosthodontic Management of a Child with Ectodermal Dysplasia: A Case Report</article-title>
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<contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Bhargava</surname>
<given-names>Akshay</given-names>
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<address><phone>+91-9312263098</phone>
<email>aksdr2000@yahoo.co.in</email>
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<xref ref-type="aff" rid="Aff1">1</xref>
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<contrib contrib-type="author"><name><surname>Sharma</surname>
<given-names>Arun</given-names>
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<contrib contrib-type="author"><name><surname>Popli</surname>
<given-names>Sachet</given-names>
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<xref ref-type="aff" rid="Aff1">1</xref>
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<contrib contrib-type="author"><name><surname>Bhargava</surname>
<given-names>Renu</given-names>
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<aff id="Aff1"><label>1</label>
Department of Prosthodontics, ITS Centre for Dental Studies and Research, Muradnagar, Ghaziabad, UP India</aff>
<aff id="Aff2"><label>2</label>
Department of Pedodontics and Preventive Dentistry, ITS Centre for Dental Studies and Research, Muradnagar, Ghaziabad, UP India</aff>
<aff id="Aff3"><label>3</label>
Raahat Dental Clinic, 285, Type-A, Pkt.-1, Sec-23, Dwarka, New Delhi, 110075 India</aff>
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<pub-date pub-type="epub"><day>8</day>
<month>12</month>
<year>2010</year>
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<pub-date pub-type="ppub"><month>6</month>
<year>2010</year>
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<volume>10</volume>
<issue>2</issue>
<fpage>137</fpage>
<lpage>140</lpage>
<history><date date-type="received"><day>13</day>
<month>7</month>
<year>2010</year>
</date>
<date date-type="accepted"><day>7</day>
<month>8</month>
<year>2010</year>
</date>
</history>
<permissions><copyright-statement>© Indian Prosthodontic Society 2010</copyright-statement>
</permissions>
<abstract id="Abs1"><p>Ectodermal dysplasia is a rare congenital disease that affects several ectodermal structures. Children with ectodermal dysplasia may have various manifestation of the disease that differ in severity and may or may not involve teeth, skin, hair, nails, sweat glands and sebaceous glands. The most common form of the ectodermal dysplasia syndrome is hypohidrotic ectodermal dysplasia and is usually inherited as an X-linked recessive trait. Female carriers may have a variable degree of clinical manifestations. This case report discusses the management of a 5-year-old girl with ectodermal dysplasia. Clinical management consisted of fabricating upper and lower dentures to help in psychosocial development and to restore the vertical dimension, esthetics and functioning of the stomatognathic system.</p>
</abstract>
<kwd-group><title>Keywords</title>
<kwd>Ectodermal dysplasia</kwd>
<kwd>Christ Siemens syndrome</kwd>
<kwd>Hypohidrosis</kwd>
<kwd>Hypotrichosis</kwd>
<kwd>Hypodontia</kwd>
</kwd-group>
<custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name>
<meta-value>© Indian Prosthodontic Society 2010</meta-value>
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