Enamel Pit Defects and Taurodontism in a Patient with Ring Chromosome 14 and 47,XXX.
Identifieur interne : 000118 ( Main/Exploration ); précédent : 000117; suivant : 000119Enamel Pit Defects and Taurodontism in a Patient with Ring Chromosome 14 and 47,XXX.
Auteurs : Janice A. Townsend [États-Unis] ; Letitia Lacour [États-Unis] ; Angela E. Scheuerle [États-Unis]Source :
- Journal of dentistry for children (Chicago, Ill.) [ 1935-5068 ] ; 2017.
Descripteurs français
- KwdFr :
- Aberrations des chromosomes sexuels (MeSH), Anesthésie générale (MeSH), Caries dentaires (imagerie diagnostique), Caries dentaires (rééducation et réadaptation), Caries dentaires (thérapie), Cavité pulpaire de la dent (malformations), Chromosomes X humains (MeSH), Chromosomes en anneau (MeSH), Chromosomes humains de la paire 14 (MeSH), Enfant (MeSH), Femelle (MeSH), Humains (MeSH), Hypoplasie de l'émail dentaire (imagerie diagnostique), Malformations dentaires (étiologie), Nouvelle-Orléans (MeSH), Stimulation du nerf vague (MeSH), Trisomie (physiopathologie), Troubles du développement sexuel avec anomalie des gonosomes (complications), Troubles du développement sexuel avec anomalie des gonosomes (physiopathologie), Émail dentaire (imagerie diagnostique), Émail dentaire (malformations), Épilepsie (MeSH).
- MESH :
- imagerie diagnostique : Caries dentaires, Hypoplasie de l'émail dentaire, Émail dentaire.
- malformations : Cavité pulpaire de la dent, Troubles du développement sexuel avec anomalie des gonosomes, Émail dentaire.
- physiopathologie : Trisomie, Troubles du développement sexuel avec anomalie des gonosomes.
- rééducation et réadaptation : Caries dentaires.
- thérapie : Caries dentaires.
- étiologie : Malformations dentaires.
- Aberrations des chromosomes sexuels, Anesthésie générale, Chromosomes X humains, Chromosomes en anneau, Chromosomes humains de la paire 14, Enfant, Femelle, Humains, Nouvelle-Orléans, Stimulation du nerf vague, Épilepsie.
English descriptors
- KwdEn :
- Anesthesia, General (MeSH), Child (MeSH), Chromosomes, Human, Pair 14 (MeSH), Chromosomes, Human, X (MeSH), Dental Caries (diagnostic imaging), Dental Caries (rehabilitation), Dental Caries (therapy), Dental Enamel (abnormalities), Dental Enamel (diagnostic imaging), Dental Enamel Hypoplasia (diagnostic imaging), Dental Pulp Cavity (abnormalities), Epilepsy (MeSH), Female (MeSH), Humans (MeSH), New Orleans (MeSH), Ring Chromosomes (MeSH), Sex Chromosome Aberrations (MeSH), Sex Chromosome Disorders of Sex Development (complications), Sex Chromosome Disorders of Sex Development (physiopathology), Tooth Abnormalities (etiology), Trisomy (physiopathology), Vagus Nerve Stimulation (MeSH).
- MESH :
- abnormalities : Dental Enamel, Dental Pulp Cavity.
- complications : Sex Chromosome Disorders of Sex Development.
- diagnostic imaging : Dental Caries, Dental Enamel, Dental Enamel Hypoplasia.
- etiology : Tooth Abnormalities.
- physiopathology : Sex Chromosome Disorders of Sex Development, Trisomy.
- rehabilitation : Dental Caries.
- therapy : Dental Caries.
- Anesthesia, General, Child, Chromosomes, Human, Pair 14, Chromosomes, Human, X, Epilepsy, Female, Humans, New Orleans, Ring Chromosomes, Sex Chromosome Aberrations, Vagus Nerve Stimulation.
Abstract
The purpose of this paper is to describe the clinical findings and management of a case involving a patient with co-occurring ring chromosome 14 syndrome and 47,XXX presenting with enamel pit defects and taurodontism. Ring chromosome 14 syndrome is an unusual condition with uncontrolled seizure disorder as its most significant finding; 47,XXX (trisomy X; triple X) is a more common condition and has characteristic physical and behavioral findings. Neither condition has been associated with enamel pit defects.
PubMed: 28387189
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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(diagnostic imaging)</term><term>Dental Caries (rehabilitation)</term><term>Dental Caries (therapy)</term><term>Dental Enamel (abnormalities)</term><term>Dental Enamel (diagnostic imaging)</term><term>Dental Enamel Hypoplasia (diagnostic imaging)</term><term>Dental Pulp Cavity (abnormalities)</term><term>Epilepsy (MeSH)</term><term>Female (MeSH)</term><term>Humans (MeSH)</term><term>New Orleans (MeSH)</term><term>Ring Chromosomes (MeSH)</term><term>Sex Chromosome Aberrations (MeSH)</term><term>Sex Chromosome Disorders of Sex Development (complications)</term><term>Sex Chromosome Disorders of Sex Development (physiopathology)</term><term>Tooth Abnormalities (etiology)</term><term>Trisomy (physiopathology)</term><term>Vagus Nerve Stimulation (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Aberrations des chromosomes sexuels (MeSH)</term><term>Anesthésie générale (MeSH)</term><term>Caries dentaires (imagerie diagnostique)</term><term>Caries dentaires (rééducation et 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Ring chromosome 14 syndrome is an unusual condition with uncontrolled seizure disorder as its most significant finding; 47,XXX (trisomy X; triple X) is a more common condition and has characteristic physical and behavioral findings. Neither condition has been associated with enamel pit defects.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">28387189</PMID><DateCompleted><Year>2018</Year><Month>03</Month><Day>06</Day></DateCompleted><DateRevised><Year>2018</Year><Month>03</Month><Day>06</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1935-5068</ISSN><JournalIssue CitedMedium="Internet"><Volume>84</Volume><Issue>1</Issue><PubDate><Year>2017</Year><Month>Jan</Month><Day>15</Day></PubDate></JournalIssue><Title>Journal of dentistry for children (Chicago, Ill.)</Title><ISOAbbreviation>J Dent Child (Chic)</ISOAbbreviation></Journal><ArticleTitle>Enamel Pit Defects and Taurodontism in a Patient with Ring Chromosome 14 and 47,XXX.</ArticleTitle><Pagination><MedlinePgn>39-43</MedlinePgn></Pagination><Abstract><AbstractText>The purpose of this paper is to describe the clinical findings and management of a case involving a patient with co-occurring ring chromosome 14 syndrome and 47,XXX presenting with enamel pit defects and taurodontism. Ring chromosome 14 syndrome is an unusual condition with uncontrolled seizure disorder as its most significant finding; 47,XXX (trisomy X; triple X) is a more common condition and has characteristic physical and behavioral findings. Neither condition has been associated with enamel pit defects.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Townsend</LastName><ForeName>Janice A</ForeName><Initials>JA</Initials><AffiliationInfo><Affiliation>Associate professor and chair, Department of Pediatric Dentistry, Louisiana State University Health Sciences Center School of Dentistry, New Orleans, La., USA;, Email: jtown2@lsuhsc.edu.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lacour</LastName><ForeName>Letitia</ForeName><Initials>L</Initials><AffiliationInfo><Affiliation>Dentist in private practice, Hammond, La., USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Scheuerle</LastName><ForeName>Angela E</ForeName><Initials>AE</Initials><AffiliationInfo><Affiliation>Professor, Department of Pediatrics, Division of Genetics and Metabolism, University of Texas Southwestern Medical Center, Dallas, Texas, USA.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Dent Child (Chic)</MedlineTA><NlmUniqueID>101180951</NlmUniqueID><ISSNLinking>1551-8949</ISSNLinking></MedlineJournalInfo><SupplMeshList><SupplMeshName Type="Disease" UI="C535487">Ring Chromosome 14 Syndrome</SupplMeshName><SupplMeshName Type="Disease" UI="C536946">Taurodontism</SupplMeshName><SupplMeshName Type="Disease" UI="C535318">Triple X syndrome</SupplMeshName></SupplMeshList><CitationSubset>D</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000768" MajorTopicYN="N">Anesthesia, General</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002648" MajorTopicYN="N">Child</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002883" MajorTopicYN="N">Chromosomes, Human, Pair 14</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D041321" MajorTopicYN="N">Chromosomes, Human, X</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003731" MajorTopicYN="N">Dental Caries</DescriptorName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName><QualifierName UI="Q000534" MajorTopicYN="N">rehabilitation</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003743" MajorTopicYN="N">Dental Enamel</DescriptorName><QualifierName UI="Q000002" MajorTopicYN="Y">abnormalities</QualifierName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003744" MajorTopicYN="N">Dental Enamel Hypoplasia</DescriptorName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003786" MajorTopicYN="N">Dental Pulp Cavity</DescriptorName><QualifierName UI="Q000002" MajorTopicYN="Y">abnormalities</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004827" MajorTopicYN="N">Epilepsy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D055820" MajorTopicYN="N">New Orleans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012303" MajorTopicYN="Y">Ring Chromosomes</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012729" MajorTopicYN="N">Sex Chromosome Aberrations</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D058533" MajorTopicYN="N">Sex Chromosome Disorders of Sex Development</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014071" MajorTopicYN="N">Tooth Abnormalities</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014314" MajorTopicYN="N">Trisomy</DescriptorName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D055536" MajorTopicYN="N">Vagus Nerve Stimulation</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2017</Year><Month>4</Month><Day>8</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2017</Year><Month>4</Month><Day>8</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2018</Year><Month>3</Month><Day>7</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">28387189</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country><region><li>Texas</li></region></list><tree><country name="États-Unis"><noRegion><name sortKey="Townsend, Janice A" sort="Townsend, Janice A" uniqKey="Townsend J" first="Janice A" last="Townsend">Janice A. Townsend</name></noRegion><name sortKey="Lacour, Letitia" sort="Lacour, Letitia" uniqKey="Lacour L" first="Letitia" last="Lacour">Letitia Lacour</name><name sortKey="Scheuerle, Angela E" sort="Scheuerle, Angela E" uniqKey="Scheuerle A" first="Angela E" last="Scheuerle">Angela E. Scheuerle</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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