The role of ultrasound in the diagnosis of fetal genetic syndromes
Identifieur interne : 002402 ( Main/Exploration ); précédent : 002401; suivant : 002403The role of ultrasound in the diagnosis of fetal genetic syndromes
Auteurs : Shayna N. Conner ; Ryan E. Longman ; Alison G. CahillSource :
- Best practice & research. Clinical obstetrics & gynaecology [ 1521-6934 ] ; 2014.
Abstract
The use of ultrasound in the prenatal diagnosis of fetal genetic syndromes is rapidly evolving. Advancing technology and new research findings are aiding in the increased accuracy of ultrasound-based diagnosis in combination with other methods of non-invasive and invasive fetal testing. Ultrasound as a screening tool for aneuploidy and other anomalies is increasingly being used throughout pregnancy, beginning in the first trimester. Given the number of recorded syndromes, it is important to identify patterns and establish a strategy for identifying abnormalities on ultrasound. These syndromes encompass a wide range of causes from viral, substance-linked, chromosomal, and other genetic syndromes. Despite the ability of those experienced in ultrasound, it is important to note that not all fetal genetic syndromes can be identified prenatally, and even common syndromes often have no associated ultrasound findings. Here, we review the role of ultrasound in the diagnosis of fetal genetic syndromes.
Url:
DOI: 10.1016/j.bpobgyn.2014.01.005
PubMed: 24534428
PubMed Central: 4079588
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Pmc, to step Corpus: 003460
- to stream Pmc, to step Curation: 003459
- to stream Pmc, to step Checkpoint: 001681
- to stream Ncbi, to step Merge: 006317
- to stream Ncbi, to step Curation: 006317
- to stream Ncbi, to step Checkpoint: 006317
- to stream Main, to step Merge: 002405
- to stream Main, to step Curation: 002402
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">The role of ultrasound in the diagnosis of fetal genetic syndromes</title><author><name sortKey="Conner, Shayna N" sort="Conner, Shayna N" uniqKey="Conner S" first="Shayna N." last="Conner">Shayna N. Conner</name></author><author><name sortKey="Longman, Ryan E" sort="Longman, Ryan E" uniqKey="Longman R" first="Ryan E." last="Longman">Ryan E. Longman</name></author><author><name sortKey="Cahill, Alison G" sort="Cahill, Alison G" uniqKey="Cahill A" first="Alison G." last="Cahill">Alison G. Cahill</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">24534428</idno><idno type="pmc">4079588</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079588</idno><idno type="RBID">PMC:4079588</idno><idno type="doi">10.1016/j.bpobgyn.2014.01.005</idno><date when="2014">2014</date><idno type="wicri:Area/Pmc/Corpus">003460</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">003460</idno><idno type="wicri:Area/Pmc/Curation">003459</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Curation">003459</idno><idno type="wicri:Area/Pmc/Checkpoint">001681</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Checkpoint">001681</idno><idno type="wicri:Area/Ncbi/Merge">006317</idno><idno type="wicri:Area/Ncbi/Curation">006317</idno><idno type="wicri:Area/Ncbi/Checkpoint">006317</idno><idno type="wicri:doubleKey">1521-6934:2014:Conner S:the:role:of</idno><idno type="wicri:Area/Main/Merge">002405</idno><idno type="wicri:Area/Main/Curation">002402</idno><idno type="wicri:Area/Main/Exploration">002402</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">The role of ultrasound in the diagnosis of fetal genetic syndromes</title><author><name sortKey="Conner, Shayna N" sort="Conner, Shayna N" uniqKey="Conner S" first="Shayna N." last="Conner">Shayna N. Conner</name></author><author><name sortKey="Longman, Ryan E" sort="Longman, Ryan E" uniqKey="Longman R" first="Ryan E." last="Longman">Ryan E. Longman</name></author><author><name sortKey="Cahill, Alison G" sort="Cahill, Alison G" uniqKey="Cahill A" first="Alison G." last="Cahill">Alison G. Cahill</name></author></analytic><series><title level="j">Best practice & research. Clinical obstetrics & gynaecology</title><idno type="ISSN">1521-6934</idno><idno type="eISSN">1532-1932</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p id="P2">The use of ultrasound in the prenatal diagnosis of fetal genetic syndromes is rapidly evolving. Advancing technology and new research findings are aiding in the increased accuracy of ultrasound-based diagnosis in combination with other methods of non-invasive and invasive fetal testing. Ultrasound as a screening tool for aneuploidy and other anomalies is increasingly being used throughout pregnancy, beginning in the first trimester. Given the number of recorded syndromes, it is important to identify patterns and establish a strategy for identifying abnormalities on ultrasound. These syndromes encompass a wide range of causes from viral, substance-linked, chromosomal, and other genetic syndromes. Despite the ability of those experienced in ultrasound, it is important to note that not all fetal genetic syndromes can be identified prenatally, and even common syndromes often have no associated ultrasound findings. Here, we review the role of ultrasound in the diagnosis of fetal genetic syndromes.</p></div></front></TEI><affiliations><list></list><tree><noCountry><name sortKey="Cahill, Alison G" sort="Cahill, Alison G" uniqKey="Cahill A" first="Alison G." last="Cahill">Alison G. Cahill</name><name sortKey="Conner, Shayna N" sort="Conner, Shayna N" uniqKey="Conner S" first="Shayna N." last="Conner">Shayna N. Conner</name><name sortKey="Longman, Ryan E" sort="Longman, Ryan E" uniqKey="Longman R" first="Ryan E." last="Longman">Ryan E. Longman</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002402 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002402 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Main
|étape= Exploration
|type= RBID
|clé= PMC:4079588
|texte= The role of ultrasound in the diagnosis of fetal genetic syndromes
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:24534428" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \
| NlmPubMed2Wicri -a LymphedemaV1
| This area was generated with Dilib version V0.6.31. |  |