Association between fetal lymphedema and congenital cardiovascular defects in Turner syndrome.
Identifieur interne : 008043 ( Main/Exploration ); précédent : 008042; suivant : 008044Association between fetal lymphedema and congenital cardiovascular defects in Turner syndrome.
Auteurs : Melissa L. Loscalzo [États-Unis] ; Phillip L. Van ; Vincent B. Ho ; Vladimir K. Bakalov ; Douglas R. Rosing ; Carol A. Malone ; Harry C. Dietz ; Carolyn A. BondySource :
- Pediatrics [ 1098-4275 ] ; 2005.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Syndrome de Turner.
- malformations : Rein, Valve aortique.
- Adulte, Coarctation aortique, Femelle, Génotype, Humains, Lymphoedème, Maladies foetales, Modèles linéaires, Phénotype, Syndrome de Turner, Études prospectives.
English descriptors
- KwdEn :
- MESH :
- abnormalities : Aortic Valve, Kidney.
- complications : Aortic Coarctation, Lymphedema, Turner Syndrome.
- genetics : Turner Syndrome.
- Adult, Female, Fetal Diseases, Genotype, Humans, Linear Models, Phenotype, Prospective Studies.
Abstract
Turner syndrome (TS) is associated with congenital cardiovascular defects (CCVDs), most commonly bicuspid aortic valve (BAV) and aortic coarctation (COARC), congenital renal anomalies, and fetal lymphedema. It has been theorized that compressive or obstructive effects of fetal lymphedema may actually cause cardiovascular and renal dysmorphogenesis in TS. The objective of this study was to determine whether there is a specific association between a history of fetal lymphedema and CCVDs in monosomy X, or TS, independent of karyotype or general severity of the phenotype.
DOI: 10.1542/peds.2004-1369
PubMed: 15741379
Affiliations:
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Le document en format XML
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Van</name></author><author><name sortKey="Ho, Vincent B" sort="Ho, Vincent B" uniqKey="Ho V" first="Vincent B" last="Ho">Vincent B. Ho</name></author><author><name sortKey="Bakalov, Vladimir K" sort="Bakalov, Vladimir K" uniqKey="Bakalov V" first="Vladimir K" last="Bakalov">Vladimir K. Bakalov</name></author><author><name sortKey="Rosing, Douglas R" sort="Rosing, Douglas R" uniqKey="Rosing D" first="Douglas R" last="Rosing">Douglas R. Rosing</name></author><author><name sortKey="Malone, Carol A" sort="Malone, Carol A" uniqKey="Malone C" first="Carol A" last="Malone">Carol A. Malone</name></author><author><name sortKey="Dietz, Harry C" sort="Dietz, Harry C" uniqKey="Dietz H" first="Harry C" last="Dietz">Harry C. Dietz</name></author><author><name sortKey="Bondy, Carolyn A" sort="Bondy, Carolyn A" uniqKey="Bondy C" first="Carolyn A" last="Bondy">Carolyn A. 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Loscalzo</name><affiliation wicri:level="2"><nlm:affiliation>McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland</wicri:regionArea><placeName><region type="state">Maryland</region></placeName></affiliation></author><author><name sortKey="Van, Phillip L" sort="Van, Phillip L" uniqKey="Van P" first="Phillip L" last="Van">Phillip L. Van</name></author><author><name sortKey="Ho, Vincent B" sort="Ho, Vincent B" uniqKey="Ho V" first="Vincent B" last="Ho">Vincent B. Ho</name></author><author><name sortKey="Bakalov, Vladimir K" sort="Bakalov, Vladimir K" uniqKey="Bakalov V" first="Vladimir K" last="Bakalov">Vladimir K. Bakalov</name></author><author><name sortKey="Rosing, Douglas R" sort="Rosing, Douglas R" uniqKey="Rosing D" first="Douglas R" last="Rosing">Douglas R. Rosing</name></author><author><name sortKey="Malone, Carol A" sort="Malone, Carol A" uniqKey="Malone C" first="Carol A" last="Malone">Carol A. Malone</name></author><author><name sortKey="Dietz, Harry C" sort="Dietz, Harry C" uniqKey="Dietz H" first="Harry C" last="Dietz">Harry C. Dietz</name></author><author><name sortKey="Bondy, Carolyn A" sort="Bondy, Carolyn A" uniqKey="Bondy C" first="Carolyn A" last="Bondy">Carolyn A. Bondy</name></author></analytic><series><title level="j">Pediatrics</title><idno type="eISSN">1098-4275</idno><imprint><date when="2005" type="published">2005</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Aortic Coarctation (complications)</term><term>Aortic Valve (abnormalities)</term><term>Female</term><term>Fetal Diseases</term><term>Genotype</term><term>Humans</term><term>Kidney (abnormalities)</term><term>Linear Models</term><term>Lymphedema (complications)</term><term>Phenotype</term><term>Prospective Studies</term><term>Turner Syndrome (complications)</term><term>Turner Syndrome (genetics)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term><term>Coarctation aortique ()</term><term>Femelle</term><term>Génotype</term><term>Humains</term><term>Lymphoedème ()</term><term>Maladies foetales</term><term>Modèles linéaires</term><term>Phénotype</term><term>Rein (malformations)</term><term>Syndrome de Turner ()</term><term>Syndrome de Turner (génétique)</term><term>Valve aortique (malformations)</term><term>Études prospectives</term></keywords><keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Aortic Valve</term><term>Kidney</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Aortic Coarctation</term><term>Lymphedema</term><term>Turner Syndrome</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Turner Syndrome</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Syndrome de Turner</term></keywords><keywords scheme="MESH" qualifier="malformations" xml:lang="fr"><term>Rein</term><term>Valve aortique</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Female</term><term>Fetal Diseases</term><term>Genotype</term><term>Humans</term><term>Linear Models</term><term>Phenotype</term><term>Prospective Studies</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte</term><term>Coarctation aortique</term><term>Femelle</term><term>Génotype</term><term>Humains</term><term>Lymphoedème</term><term>Maladies foetales</term><term>Modèles linéaires</term><term>Phénotype</term><term>Syndrome de Turner</term><term>Études prospectives</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Turner syndrome (TS) is associated with congenital cardiovascular defects (CCVDs), most commonly bicuspid aortic valve (BAV) and aortic coarctation (COARC), congenital renal anomalies, and fetal lymphedema. It has been theorized that compressive or obstructive effects of fetal lymphedema may actually cause cardiovascular and renal dysmorphogenesis in TS. The objective of this study was to determine whether there is a specific association between a history of fetal lymphedema and CCVDs in monosomy X, or TS, independent of karyotype or general severity of the phenotype.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>Maryland</li></region></list><tree><noCountry><name sortKey="Bakalov, Vladimir K" sort="Bakalov, Vladimir K" uniqKey="Bakalov V" first="Vladimir K" last="Bakalov">Vladimir K. Bakalov</name><name sortKey="Bondy, Carolyn A" sort="Bondy, Carolyn A" uniqKey="Bondy C" first="Carolyn A" last="Bondy">Carolyn A. Bondy</name><name sortKey="Dietz, Harry C" sort="Dietz, Harry C" uniqKey="Dietz H" first="Harry C" last="Dietz">Harry C. Dietz</name><name sortKey="Ho, Vincent B" sort="Ho, Vincent B" uniqKey="Ho V" first="Vincent B" last="Ho">Vincent B. Ho</name><name sortKey="Malone, Carol A" sort="Malone, Carol A" uniqKey="Malone C" first="Carol A" last="Malone">Carol A. Malone</name><name sortKey="Rosing, Douglas R" sort="Rosing, Douglas R" uniqKey="Rosing D" first="Douglas R" last="Rosing">Douglas R. Rosing</name><name sortKey="Van, Phillip L" sort="Van, Phillip L" uniqKey="Van P" first="Phillip L" last="Van">Phillip L. Van</name></noCountry><country name="États-Unis"><region name="Maryland"><name sortKey="Loscalzo, Melissa L" sort="Loscalzo, Melissa L" uniqKey="Loscalzo M" first="Melissa L" last="Loscalzo">Melissa L. Loscalzo</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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