LymphedemaV1, PubMed, Checkpoint, bibRecord, 005C19

[Fetal neck edema--early sonographic indications of a chromosome abnormality].

Identifieur interne : 005C19 ( PubMed/Checkpoint ); précédent : 005C18; suivant : 005C20

[Fetal neck edema--early sonographic indications of a chromosome abnormality].

Auteurs : H J Voigt ; U. Claussen ; R. Ulmer

Source :

Geburtshilfe und Frauenheilkunde [ 0016-5751 ] ; 1986.

RBID : pubmed:2950017

Descripteurs français

KwdFr :
- Aberrations des chromosomes (diagnostic), Aberrations des chromosomes (génétique), Adulte, Avortement provoqué, Caryotypage, Cou (malformations), Diagnostic prénatal, Femelle, Grossesse, Humains, Lymphoedème (diagnostic), Lymphoedème (génétique), Maladies chromosomiques, Mâle, Nouveau-né, Syndrome de Down (génétique), Syndrome de Turner (génétique), Système lymphatique (malformations), Échographie.
MESH :
- diagnostic : Aberrations des chromosomes, Lymphoedème.
- génétique : Aberrations des chromosomes, Lymphoedème, Syndrome de Down, Syndrome de Turner.
- malformations : Cou, Système lymphatique.
- Adulte, Avortement provoqué, Caryotypage, Diagnostic prénatal, Femelle, Grossesse, Humains, Maladies chromosomiques, Mâle, Nouveau-né, Échographie.

English descriptors

KwdEn :
- Abortion, Induced, Adult, Chromosome Aberrations (diagnosis), Chromosome Aberrations (genetics), Chromosome Disorders, Down Syndrome (genetics), Female, Humans, Infant, Newborn, Karyotyping, Lymphatic System (abnormalities), Lymphedema (diagnosis), Lymphedema (genetics), Male, Neck (abnormalities), Pregnancy, Prenatal Diagnosis, Turner Syndrome (genetics), Ultrasonography.
MESH :
- abnormalities : Lymphatic System, Neck.
- diagnosis : Chromosome Aberrations, Lymphedema.
- genetics : Chromosome Aberrations, Down Syndrome, Lymphedema, Turner Syndrome.
- Abortion, Induced, Adult, Chromosome Disorders, Female, Humans, Infant, Newborn, Karyotyping, Male, Pregnancy, Prenatal Diagnosis, Ultrasonography.

Abstract

Fetal nuchal edema is described as an early sonographic sign of a chromosomal anomaly. Eight cases of fetal nuchal edema were detected by sonography, and for this reason the fetal karyotypes were established by means of rapid karyotyping. Trisomy 21 (Down's syndrome) and the 45,XO constellation (Turner's syndrome) were most commonly found. In one case with trisomy 21, only a temporary occurrence of fetal nuchal edema could be identified. The pathogenesis of fetal edemas is discussed. If the likelihood of pathologic conditions can be ruled out by sonography, differentiated counseling for antenatal diagnosis is possible.

DOI: 10.1055/s-2008-1036338
PubMed: 2950017

Affiliations:

Links toward previous steps (curation, corpus...)

to stream PubMed, to step Corpus: 006516
to stream PubMed, to step Curation: 006516

Links to Exploration step

pubmed:2950017

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">[Fetal neck edema--early sonographic indications of a chromosome abnormality].</title>
<author><name sortKey="Voigt, H J" sort="Voigt, H J" uniqKey="Voigt H" first="H J" last="Voigt">H J Voigt</name>
</author>
<author><name sortKey="Claussen, U" sort="Claussen, U" uniqKey="Claussen U" first="U" last="Claussen">U. Claussen</name>
</author>
<author><name sortKey="Ulmer, R" sort="Ulmer, R" uniqKey="Ulmer R" first="R" last="Ulmer">R. Ulmer</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1986">1986</date>
<idno type="RBID">pubmed:2950017</idno>
<idno type="pmid">2950017</idno>
<idno type="doi">10.1055/s-2008-1036338</idno>
<idno type="wicri:Area/PubMed/Corpus">006516</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">006516</idno>
<idno type="wicri:Area/PubMed/Curation">006516</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">006516</idno>
<idno type="wicri:Area/PubMed/Checkpoint">006516</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">006516</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">[Fetal neck edema--early sonographic indications of a chromosome abnormality].</title>
<author><name sortKey="Voigt, H J" sort="Voigt, H J" uniqKey="Voigt H" first="H J" last="Voigt">H J Voigt</name>
</author>
<author><name sortKey="Claussen, U" sort="Claussen, U" uniqKey="Claussen U" first="U" last="Claussen">U. Claussen</name>
</author>
<author><name sortKey="Ulmer, R" sort="Ulmer, R" uniqKey="Ulmer R" first="R" last="Ulmer">R. Ulmer</name>
</author>
</analytic>
<series><title level="j">Geburtshilfe und Frauenheilkunde</title>
<idno type="ISSN">0016-5751</idno>
<imprint><date when="1986" type="published">1986</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Abortion, Induced</term>
<term>Adult</term>
<term>Chromosome Aberrations (diagnosis)</term>
<term>Chromosome Aberrations (genetics)</term>
<term>Chromosome Disorders</term>
<term>Down Syndrome (genetics)</term>
<term>Female</term>
<term>Humans</term>
<term>Infant, Newborn</term>
<term>Karyotyping</term>
<term>Lymphatic System (abnormalities)</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (genetics)</term>
<term>Male</term>
<term>Neck (abnormalities)</term>
<term>Pregnancy</term>
<term>Prenatal Diagnosis</term>
<term>Turner Syndrome (genetics)</term>
<term>Ultrasonography</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Aberrations des chromosomes (diagnostic)</term>
<term>Aberrations des chromosomes (génétique)</term>
<term>Adulte</term>
<term>Avortement provoqué</term>
<term>Caryotypage</term>
<term>Cou (malformations)</term>
<term>Diagnostic prénatal</term>
<term>Femelle</term>
<term>Grossesse</term>
<term>Humains</term>
<term>Lymphoedème (diagnostic)</term>
<term>Lymphoedème (génétique)</term>
<term>Maladies chromosomiques</term>
<term>Mâle</term>
<term>Nouveau-né</term>
<term>Syndrome de Down (génétique)</term>
<term>Syndrome de Turner (génétique)</term>
<term>Système lymphatique (malformations)</term>
<term>Échographie</term>
</keywords>
<keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Lymphatic System</term>
<term>Neck</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Chromosome Aberrations</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Aberrations des chromosomes</term>
<term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chromosome Aberrations</term>
<term>Down Syndrome</term>
<term>Lymphedema</term>
<term>Turner Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Aberrations des chromosomes</term>
<term>Lymphoedème</term>
<term>Syndrome de Down</term>
<term>Syndrome de Turner</term>
</keywords>
<keywords scheme="MESH" qualifier="malformations" xml:lang="fr"><term>Cou</term>
<term>Système lymphatique</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Abortion, Induced</term>
<term>Adult</term>
<term>Chromosome Disorders</term>
<term>Female</term>
<term>Humans</term>
<term>Infant, Newborn</term>
<term>Karyotyping</term>
<term>Male</term>
<term>Pregnancy</term>
<term>Prenatal Diagnosis</term>
<term>Ultrasonography</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adulte</term>
<term>Avortement provoqué</term>
<term>Caryotypage</term>
<term>Diagnostic prénatal</term>
<term>Femelle</term>
<term>Grossesse</term>
<term>Humains</term>
<term>Maladies chromosomiques</term>
<term>Mâle</term>
<term>Nouveau-né</term>
<term>Échographie</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Fetal nuchal edema is described as an early sonographic sign of a chromosomal anomaly. Eight cases of fetal nuchal edema were detected by sonography, and for this reason the fetal karyotypes were established by means of rapid karyotyping. Trisomy 21 (Down's syndrome) and the 45,XO constellation (Turner's syndrome) were most commonly found. In one case with trisomy 21, only a temporary occurrence of fetal nuchal edema could be identified. The pathogenesis of fetal edemas is discussed. If the likelihood of pathologic conditions can be ruled out by sonography, differentiated counseling for antenatal diagnosis is possible.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">2950017</PMID>
<DateCreated><Year>1987</Year>
<Month>04</Month>
<Day>13</Day>
</DateCreated>
<DateCompleted><Year>1987</Year>
<Month>04</Month>
<Day>13</Day>
</DateCompleted>
<DateRevised><Year>2006</Year>
<Month>11</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0016-5751</ISSN>
<JournalIssue CitedMedium="Print"><Volume>46</Volume>
<Issue>12</Issue>
<PubDate><Year>1986</Year>
<Month>Dec</Month>
</PubDate>
</JournalIssue>
<Title>Geburtshilfe und Frauenheilkunde</Title>
<ISOAbbreviation>Geburtshilfe Frauenheilkd</ISOAbbreviation>
</Journal>
<ArticleTitle>[Fetal neck edema--early sonographic indications of a chromosome abnormality].</ArticleTitle>
<Pagination><MedlinePgn>879-82</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Fetal nuchal edema is described as an early sonographic sign of a chromosomal anomaly. Eight cases of fetal nuchal edema were detected by sonography, and for this reason the fetal karyotypes were established by means of rapid karyotyping. Trisomy 21 (Down's syndrome) and the 45,XO constellation (Turner's syndrome) were most commonly found. In one case with trisomy 21, only a temporary occurrence of fetal nuchal edema could be identified. The pathogenesis of fetal edemas is discussed. If the likelihood of pathologic conditions can be ruled out by sonography, differentiated counseling for antenatal diagnosis is possible.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Voigt</LastName>
<ForeName>H J</ForeName>
<Initials>HJ</Initials>
</Author>
<Author ValidYN="Y"><LastName>Claussen</LastName>
<ForeName>U</ForeName>
<Initials>U</Initials>
</Author>
<Author ValidYN="Y"><LastName>Ulmer</LastName>
<ForeName>R</ForeName>
<Initials>R</Initials>
</Author>
</AuthorList>
<Language>ger</Language>
<PublicationTypeList><PublicationType UI="D004740">English Abstract</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<VernacularTitle>Das fetale Nackenödem--früher sonographischer Hinweis auf eine Chromosomenanomalie.</VernacularTitle>
</Article>
<MedlineJournalInfo><Country>Germany</Country>
<MedlineTA>Geburtshilfe Frauenheilkd</MedlineTA>
<NlmUniqueID>0370732</NlmUniqueID>
<ISSNLinking>0016-5751</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000028" MajorTopicYN="N">Abortion, Induced</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002869" MajorTopicYN="N">Chromosome Aberrations</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D025063" MajorTopicYN="N">Chromosome Disorders</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004314" MajorTopicYN="N">Down Syndrome</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007231" MajorTopicYN="N">Infant, Newborn</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007621" MajorTopicYN="N">Karyotyping</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008208" MajorTopicYN="N">Lymphatic System</DescriptorName>
<QualifierName UI="Q000002" MajorTopicYN="N">abnormalities</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009333" MajorTopicYN="N">Neck</DescriptorName>
<QualifierName UI="Q000002" MajorTopicYN="Y">abnormalities</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011247" MajorTopicYN="N">Pregnancy</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011296" MajorTopicYN="Y">Prenatal Diagnosis</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014424" MajorTopicYN="N">Turner Syndrome</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014463" MajorTopicYN="Y">Ultrasonography</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1986</Year>
<Month>12</Month>
<Day>1</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>1986</Year>
<Month>12</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>1</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>1986</Year>
<Month>12</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">2950017</ArticleId>
<ArticleId IdType="doi">10.1055/s-2008-1036338</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list></list>
<tree><noCountry><name sortKey="Claussen, U" sort="Claussen, U" uniqKey="Claussen U" first="U" last="Claussen">U. Claussen</name>
<name sortKey="Ulmer, R" sort="Ulmer, R" uniqKey="Ulmer R" first="R" last="Ulmer">R. Ulmer</name>
<name sortKey="Voigt, H J" sort="Voigt, H J" uniqKey="Voigt H" first="H J" last="Voigt">H J Voigt</name>
</noCountry>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/PubMed/Checkpoint

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 005C19 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd -nk 005C19 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    LymphedemaV1
   |flux=    PubMed
   |étape=   Checkpoint
   |type=    RBID
   |clé=     pubmed:2950017
   |texte=   [Fetal neck edema--early sonographic indications of a chromosome abnormality].
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i   -Sk "pubmed:2950017" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd   \
       | NlmPubMed2Wicri -a LymphedemaV1

This area was generated with Dilib version V0.6.31.
Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024

	Serveur d'exploration sur le lymphœdème
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Serveur d'exploration sur le lymphœdème

[Fetal neck edema--early sonographic indications of a chromosome abnormality].

[Fetal neck edema--early sonographic indications of a chromosome abnormality].

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki