[Association of aplasia cutis congenita with coarctation of the aorta: a coincidence?].
Identifieur interne : 000402 ( PubMed/Corpus ); précédent : 000401; suivant : 000403[Association of aplasia cutis congenita with coarctation of the aorta: a coincidence?].
Auteurs : H. Bruel ; J. Poinsot ; J P Chabrolle ; V. LayetSource :
- Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [ 0929-693X ] ; 1999.
English descriptors
- KwdEn :
- MESH :
- complications : Aortic Coarctation, Ectodermal Dysplasia.
- genetics : Aortic Coarctation, Ectodermal Dysplasia.
- pathology : Aortic Coarctation, Ectodermal Dysplasia.
- Female, Genetic Predisposition to Disease, Humans, Infant, Newborn.
Abstract
The association of aplasia cutis congenita and aortic coarctation could be a coincidence.
PubMed: 10587744
Links to Exploration step
pubmed:10587744Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">[Association of aplasia cutis congenita with coarctation of the aorta: a coincidence?].</title>
<author><name sortKey="Bruel, H" sort="Bruel, H" uniqKey="Bruel H" first="H" last="Bruel">H. Bruel</name>
<affiliation><nlm:affiliation>Service de médecine néonatale, centre hospitalier du Havre, Le Havre, France.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Poinsot, J" sort="Poinsot, J" uniqKey="Poinsot J" first="J" last="Poinsot">J. Poinsot</name>
</author>
<author><name sortKey="Chabrolle, J P" sort="Chabrolle, J P" uniqKey="Chabrolle J" first="J P" last="Chabrolle">J P Chabrolle</name>
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<author><name sortKey="Layet, V" sort="Layet, V" uniqKey="Layet V" first="V" last="Layet">V. Layet</name>
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<idno type="RBID">pubmed:10587744</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">[Association of aplasia cutis congenita with coarctation of the aorta: a coincidence?].</title>
<author><name sortKey="Bruel, H" sort="Bruel, H" uniqKey="Bruel H" first="H" last="Bruel">H. Bruel</name>
<affiliation><nlm:affiliation>Service de médecine néonatale, centre hospitalier du Havre, Le Havre, France.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Poinsot, J" sort="Poinsot, J" uniqKey="Poinsot J" first="J" last="Poinsot">J. Poinsot</name>
</author>
<author><name sortKey="Chabrolle, J P" sort="Chabrolle, J P" uniqKey="Chabrolle J" first="J P" last="Chabrolle">J P Chabrolle</name>
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<author><name sortKey="Layet, V" sort="Layet, V" uniqKey="Layet V" first="V" last="Layet">V. Layet</name>
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<series><title level="j">Archives de pediatrie : organe officiel de la Societe francaise de pediatrie</title>
<idno type="ISSN">0929-693X</idno>
<imprint><date when="1999" type="published">1999</date>
</imprint>
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</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aortic Coarctation (complications)</term>
<term>Aortic Coarctation (genetics)</term>
<term>Aortic Coarctation (pathology)</term>
<term>Ectodermal Dysplasia (complications)</term>
<term>Ectodermal Dysplasia (genetics)</term>
<term>Ectodermal Dysplasia (pathology)</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Humans</term>
<term>Infant, Newborn</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Aortic Coarctation</term>
<term>Ectodermal Dysplasia</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Aortic Coarctation</term>
<term>Ectodermal Dysplasia</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Aortic Coarctation</term>
<term>Ectodermal Dysplasia</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Humans</term>
<term>Infant, Newborn</term>
</keywords>
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</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">The association of aplasia cutis congenita and aortic coarctation could be a coincidence.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">10587744</PMID>
<DateCreated><Year>1999</Year>
<Month>12</Month>
<Day>28</Day>
</DateCreated>
<DateCompleted><Year>1999</Year>
<Month>12</Month>
<Day>28</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>5</Month>
<Day>20</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0929-693X</ISSN>
<JournalIssue CitedMedium="Print"><Volume>6</Volume>
<Issue>11</Issue>
<PubDate><Year>1999</Year>
<Month>Nov</Month>
</PubDate>
</JournalIssue>
<Title>Archives de pediatrie : organe officiel de la Societe francaise de pediatrie</Title>
<ISOAbbreviation>Arch Pediatr</ISOAbbreviation>
</Journal>
<ArticleTitle>[Association of aplasia cutis congenita with coarctation of the aorta: a coincidence?].</ArticleTitle>
<Pagination><MedlinePgn>1193-5</MedlinePgn>
</Pagination>
<Abstract><AbstractText Label="UNLABELLED">The association of aplasia cutis congenita and aortic coarctation could be a coincidence.</AbstractText>
<AbstractText Label="CASE REPORT" NlmCategory="METHODS">A neonate was born with an aplasia cutis congenita in the midline of the scalp. When she was two months old, an aortie coarctation was detected and surgically resected. Spontaneously, the scalp gradually cicatrized.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">A search for a candidate gene in this second reported case is mandated.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Bruel</LastName>
<ForeName>H</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Service de médecine néonatale, centre hospitalier du Havre, Le Havre, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Poinsot</LastName>
<ForeName>J</ForeName>
<Initials>J</Initials>
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<Author ValidYN="Y"><LastName>Chabrolle</LastName>
<ForeName>J P</ForeName>
<Initials>JP</Initials>
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<Author ValidYN="Y"><LastName>Layet</LastName>
<ForeName>V</ForeName>
<Initials>V</Initials>
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<VernacularTitle>Association d'une aplasie cutanée congénitale et d'une coarctation de l'aorte: association fortuite?</VernacularTitle>
</Article>
<MedlineJournalInfo><Country>France</Country>
<MedlineTA>Arch Pediatr</MedlineTA>
<NlmUniqueID>9421356</NlmUniqueID>
<ISSNLinking>0929-693X</ISSNLinking>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D001017" MajorTopicYN="N">Aortic Coarctation</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004476" MajorTopicYN="N">Ectodermal Dysplasia</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D020022" MajorTopicYN="N">Genetic Predisposition to Disease</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007231" MajorTopicYN="N">Infant, Newborn</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1999</Year>
<Month>12</Month>
<Day>10</Day>
<Hour>9</Hour>
<Minute>0</Minute>
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<PubMedPubDate PubStatus="medline"><Year>2000</Year>
<Month>5</Month>
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<PubMedPubDate PubStatus="entrez"><Year>1999</Year>
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<ArticleIdList><ArticleId IdType="pubmed">10587744</ArticleId>
<ArticleId IdType="pii">S0929693X00863034</ArticleId>
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