Lymphedema combined with brachydactyly and tachycardia
Identifieur interne : 00B670 ( Main/Exploration ); précédent : 00B669; suivant : 00B671Lymphedema combined with brachydactyly and tachycardia
Auteurs : C. Stoll [France] ; Y. Alembik [France] ; B. Dott [France] ; P. Kieffer [France]Source :
- Genetic counseling [ 1015-8146 ] ; 1998.
Descripteurs français
- KwdFr :
- Adulte, Anomalies morphologiques congénitales de la main (diagnostic), Anomalies morphologiques congénitales de la main (génétique), Doigts (malformations), Femelle, Humains, Lymphoedème (diagnostic), Lymphoedème (génétique), Phénotype, Tachycardie paroxystique (diagnostic), Tachycardie paroxystique (génétique).
- MESH :
- diagnostic : Anomalies morphologiques congénitales de la main, Lymphoedème, Tachycardie paroxystique.
- génétique : Anomalies morphologiques congénitales de la main, Lymphoedème, Tachycardie paroxystique.
- malformations : Doigts.
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Brachydactyly, Case study, Female, Finger, Fingers (abnormalities), Genetic disease, Hand Deformities, Congenital (diagnosis), Hand Deformities, Congenital (genetics), Human, Humans, Lymphedema, Lymphedema (diagnosis), Lymphedema (genetics), Phenotype, Tachycardia, Tachycardia, Paroxysmal (diagnosis), Tachycardia, Paroxysmal (genetics), Upper limb.
- MESH :
- abnormalities : Fingers.
- diagnosis : Hand Deformities, Congenital, Lymphedema, Tachycardia, Paroxysmal.
- genetics : Hand Deformities, Congenital, Lymphedema, Tachycardia, Paroxysmal.
- Adult, Female, Humans, Phenotype.
Abstract
Lymphedema combined with brachydactyly and tachycardia: Hereditary lymphedema can appear at birth or later up to adulthood. It may be seen in connection with diverse symptoms forming various syndromes. The authors report a family with hereditary lymphedema, brachydactyly, syndactyly and tachycardia. Lymphedema and tachycardia could appear together by chance. However this combination could also be a syndrome.
Affiliations:
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Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Lymphedema combined with brachydactyly and tachycardia</title>
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<series><title level="j" type="main">Genetic counseling</title>
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<seriesStmt><title level="j" type="main">Genetic counseling</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Brachydactyly</term>
<term>Case study</term>
<term>Female</term>
<term>Finger</term>
<term>Fingers (abnormalities)</term>
<term>Genetic disease</term>
<term>Hand Deformities, Congenital (diagnosis)</term>
<term>Hand Deformities, Congenital (genetics)</term>
<term>Human</term>
<term>Humans</term>
<term>Lymphedema</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (genetics)</term>
<term>Phenotype</term>
<term>Tachycardia</term>
<term>Tachycardia, Paroxysmal (diagnosis)</term>
<term>Tachycardia, Paroxysmal (genetics)</term>
<term>Upper limb</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term>
<term>Anomalies morphologiques congénitales de la main (diagnostic)</term>
<term>Anomalies morphologiques congénitales de la main (génétique)</term>
<term>Doigts (malformations)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphoedème (diagnostic)</term>
<term>Lymphoedème (génétique)</term>
<term>Phénotype</term>
<term>Tachycardie paroxystique (diagnostic)</term>
<term>Tachycardie paroxystique (génétique)</term>
</keywords>
<keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Fingers</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Hand Deformities, Congenital</term>
<term>Lymphedema</term>
<term>Tachycardia, Paroxysmal</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Anomalies morphologiques congénitales de la main</term>
<term>Lymphoedème</term>
<term>Tachycardie paroxystique</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Hand Deformities, Congenital</term>
<term>Lymphedema</term>
<term>Tachycardia, Paroxysmal</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Anomalies morphologiques congénitales de la main</term>
<term>Lymphoedème</term>
<term>Tachycardie paroxystique</term>
</keywords>
<keywords scheme="MESH" qualifier="malformations" xml:lang="fr"><term>Doigts</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Female</term>
<term>Humans</term>
<term>Phenotype</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Adulte</term>
<term>Femelle</term>
<term>Homme</term>
<term>Humains</term>
<term>Maladie héréditaire</term>
<term>Phénotype</term>
<term>Etude cas</term>
<term>Tachycardie</term>
<term>Brachydactylie</term>
<term>Membre supérieur</term>
<term>Lymphoedème</term>
<term>Doigt</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
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<front><div type="abstract" xml:lang="en">Lymphedema combined with brachydactyly and tachycardia: Hereditary lymphedema can appear at birth or later up to adulthood. It may be seen in connection with diverse symptoms forming various syndromes. The authors report a family with hereditary lymphedema, brachydactyly, syndactyly and tachycardia. Lymphedema and tachycardia could appear together by chance. However this combination could also be a syndrome.</div>
</front>
</TEI>
<affiliations><list><country><li>France</li>
</country>
<region><li>Alsace (région administrative)</li>
<li>Grand Est</li>
</region>
<settlement><li>Strasbourg</li>
</settlement>
</list>
<tree><country name="France"><region name="Grand Est"><name sortKey="Stoll, C" sort="Stoll, C" uniqKey="Stoll C" first="C." last="Stoll">C. Stoll</name>
</region>
<name sortKey="Alembik, Y" sort="Alembik, Y" uniqKey="Alembik Y" first="Y." last="Alembik">Y. Alembik</name>
<name sortKey="Dott, B" sort="Dott, B" uniqKey="Dott B" first="B." last="Dott">B. Dott</name>
<name sortKey="Kieffer, P" sort="Kieffer, P" uniqKey="Kieffer P" first="P." last="Kieffer">P. Kieffer</name>
</country>
</tree>
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</record>
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