Prenatal diagnosis of the Klippel‐Trenaunay‐Weber syndrome
Identifieur interne : 00D389 ( Main/Merge ); précédent : 00D388; suivant : 00D390Prenatal diagnosis of the Klippel‐Trenaunay‐Weber syndrome
Auteurs : Ronald J. Jorgenson [États-Unis] ; Byron Darby [États-Unis] ; Robert Patterson [États-Unis] ; Kenneth J. Trimmer [États-Unis]Source :
- Prenatal Diagnosis [ 0197-3851 ] ; 1994-10.
Abstract
The Klippel‐Trenaunay‐Weber syndrome is a complex developmental disorder of the vascular and skeletal systems. While many features of the syndrome are congenital, it has not been diagnosed often before birth. This paper describes a case of Klippel‐Trenaunay‐Weber syndrome diagnosed at 19 weeks' gestation on the basis of sonographic findings and family history. The clinical variability of the syndrome is emphasized and the importance of family history in differential diagnosis is stressed.
Url:
DOI: 10.1002/pd.1970141015
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 002131
- to stream Istex, to step Curation: 002131
- to stream Istex, to step Checkpoint: 004B09
Links to Exploration step
ISTEX:488665F79CB1F12A946E60EAAD6079CB4636C28ELe document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Prenatal diagnosis of the Klippel‐Trenaunay‐Weber syndrome</title><author><name sortKey="Jorgenson, Ronald J" sort="Jorgenson, Ronald J" uniqKey="Jorgenson R" first="Ronald J." last="Jorgenson">Ronald J. Jorgenson</name></author><author><name sortKey="Darby, Byron" sort="Darby, Byron" uniqKey="Darby B" first="Byron" last="Darby">Byron Darby</name></author><author><name sortKey="Patterson, Robert" sort="Patterson, Robert" uniqKey="Patterson R" first="Robert" last="Patterson">Robert Patterson</name></author><author><name sortKey="Trimmer, Kenneth J" sort="Trimmer, Kenneth J" uniqKey="Trimmer K" first="Kenneth J." last="Trimmer">Kenneth J. Trimmer</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:488665F79CB1F12A946E60EAAD6079CB4636C28E</idno><date when="1994" year="1994">1994</date><idno type="doi">10.1002/pd.1970141015</idno><idno type="url">https://api.istex.fr/document/488665F79CB1F12A946E60EAAD6079CB4636C28E/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">002131</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">002131</idno><idno type="wicri:Area/Istex/Curation">002131</idno><idno type="wicri:Area/Istex/Checkpoint">004B09</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">004B09</idno><idno type="wicri:doubleKey">0197-3851:1994:Jorgenson R:prenatal:diagnosis:of</idno><idno type="wicri:Area/Main/Merge">00D389</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Prenatal diagnosis of the Klippel‐Trenaunay‐Weber syndrome</title><author><name sortKey="Jorgenson, Ronald J" sort="Jorgenson, Ronald J" uniqKey="Jorgenson R" first="Ronald J." last="Jorgenson">Ronald J. Jorgenson</name><affiliation wicri:level="2"><country xml:lang="fr" wicri:curation="lc">États-Unis</country><wicri:regionArea>Central Texas Genetics Center, Austin, Texas</wicri:regionArea><placeName><region type="state">Texas</region></placeName></affiliation><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Central Texas Genetics Center, 4201 Marathon Blvd, Suite 206, Austin, TX 78756</wicri:regionArea><placeName><region type="state">Texas</region></placeName></affiliation></author><author><name sortKey="Darby, Byron" sort="Darby, Byron" uniqKey="Darby B" first="Byron" last="Darby">Byron Darby</name><affiliation wicri:level="2"><country xml:lang="fr" wicri:curation="lc">États-Unis</country><wicri:regionArea>Central Texas Perinatal Associates, Austin, Texas</wicri:regionArea><placeName><region type="state">Texas</region></placeName></affiliation></author><author><name sortKey="Patterson, Robert" sort="Patterson, Robert" uniqKey="Patterson R" first="Robert" last="Patterson">Robert Patterson</name><affiliation wicri:level="2"><country xml:lang="fr" wicri:curation="lc">États-Unis</country><wicri:regionArea>Central Texas Perinatal Associates, Austin, Texas</wicri:regionArea><placeName><region type="state">Texas</region></placeName></affiliation></author><author><name sortKey="Trimmer, Kenneth J" sort="Trimmer, Kenneth J" uniqKey="Trimmer K" first="Kenneth J." last="Trimmer">Kenneth J. Trimmer</name><affiliation wicri:level="2"><country xml:lang="fr" wicri:curation="lc">États-Unis</country><wicri:regionArea>North Texas Perinatal Associates, Dallas, Texas</wicri:regionArea><placeName><region type="state">Texas</region></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Prenatal Diagnosis</title><title level="j" type="alt">PRENATAL DIAGNOSIS</title><idno type="ISSN">0197-3851</idno><idno type="eISSN">1097-0223</idno><imprint><biblScope unit="vol">14</biblScope><biblScope unit="issue">10</biblScope><biblScope unit="page" from="989">989</biblScope><biblScope unit="page" to="992">992</biblScope><biblScope unit="page-count">4</biblScope><publisher>John Wiley & Sons, Ltd.</publisher><pubPlace>Chichester, UK</pubPlace><date type="published" when="1994-10">1994-10</date></imprint><idno type="ISSN">0197-3851</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0197-3851</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The Klippel‐Trenaunay‐Weber syndrome is a complex developmental disorder of the vascular and skeletal systems. While many features of the syndrome are congenital, it has not been diagnosed often before birth. This paper describes a case of Klippel‐Trenaunay‐Weber syndrome diagnosed at 19 weeks' gestation on the basis of sonographic findings and family history. The clinical variability of the syndrome is emphasized and the importance of family history in differential diagnosis is stressed.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 00D389 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Merge/biblio.hfd -nk 00D389 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Main
|étape= Merge
|type= RBID
|clé= ISTEX:488665F79CB1F12A946E60EAAD6079CB4636C28E
|texte= Prenatal diagnosis of the Klippel‐Trenaunay‐Weber syndrome
}}
| This area was generated with Dilib version V0.6.31. |  |