LymphedemaV1, PubMed, Curation, bibRecord, 000A82

A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE.

Identifieur interne : 000A82 ( PubMed/Curation ); précédent : 000A81; suivant : 000A83

A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE.

Auteurs : N F Liu ; Z. Yu ; Y. Luo ; D. Sun ; Z. Yan

Source :

Lymphology [ 0024-7766 ] ; 2015.

RBID : pubmed:26714373

Descripteurs français

KwdFr :
- Adulte, Analyse de mutations d'ADN, Chine, Enfant d'âge préscolaire, Femelle, Humains, Hérédité, Imagerie par résonance magnétique, Lymphoedème (anatomopathologie), Lymphoedème (ethnologie), Lymphoedème (génétique), Lymphographie (), Membre inférieur (anatomopathologie), Mutation, Mâle, Pedigree, Phénotype, Population d'origine asiatique (génétique), Prédisposition génétique à une maladie, Récepteur-3 au facteur croissance endothéliale vasculaire (génétique), Valeur prédictive des tests.
MESH :
- anatomopathologie : Lymphoedème, Membre inférieur.
- ethnologie : Lymphoedème.
- génétique : Lymphoedème, Population d'origine asiatique, Récepteur-3 au facteur croissance endothéliale vasculaire.
- Adulte, Analyse de mutations d'ADN, Chine, Enfant d'âge préscolaire, Femelle, Humains, Hérédité, Imagerie par résonance magnétique, Lymphographie, Mutation, Mâle, Pedigree, Phénotype, Prédisposition génétique à une maladie, Valeur prédictive des tests.

English descriptors

KwdEn :
- Adult, Asian Continental Ancestry Group (genetics), Child, Preschool, China, DNA Mutational Analysis, Female, Genetic Predisposition to Disease, Heredity, Humans, Lower Extremity (pathology), Lymphedema (ethnology), Lymphedema (genetics), Lymphedema (pathology), Lymphography (methods), Magnetic Resonance Imaging, Male, Mutation, Pedigree, Phenotype, Predictive Value of Tests, Vascular Endothelial Growth Factor Receptor-3 (genetics).
MESH :
- chemical , genetics : Vascular Endothelial Growth Factor Receptor-3.
- ethnology : Lymphedema.
- genetics : Asian Continental Ancestry Group, Lymphedema.
- methods : Lymphography.
- pathology : Lower Extremity, Lymphedema.
- Adult, Child, Preschool, China, DNA Mutational Analysis, Female, Genetic Predisposition to Disease, Heredity, Humans, Magnetic Resonance Imaging, Male, Mutation, Pedigree, Phenotype, Predictive Value of Tests.

Abstract

Milroy disease is a congenital onset lymphedema linked to FLT4 gene mutations in the tyrosine kinase domain. So far, a total of 59 different FLT4 variants have been identified. Here, we report a novel FLT4 gene mutation in a Chinese family with Milroy disease and present their clinical symptoms and MR lymphangiographic findings.

PubMed: 26714373

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Le document en format XML

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<author><name sortKey="Yu, Z" sort="Yu, Z" uniqKey="Yu Z" first="Z" last="Yu">Z. Yu</name>
</author>
<author><name sortKey="Luo, Y" sort="Luo, Y" uniqKey="Luo Y" first="Y" last="Luo">Y. Luo</name>
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<author><name sortKey="Sun, D" sort="Sun, D" uniqKey="Sun D" first="D" last="Sun">D. Sun</name>
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<author><name sortKey="Yan, Z" sort="Yan, Z" uniqKey="Yan Z" first="Z" last="Yan">Z. Yan</name>
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<term>Genetic Predisposition to Disease</term>
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<term>Humains</term>
<term>Hérédité</term>
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<term>Valeur prédictive des tests</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Vascular Endothelial Growth Factor Receptor-3</term>
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<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Lymphoedème</term>
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<term>Predictive Value of Tests</term>
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<term>Analyse de mutations d'ADN</term>
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<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
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<term>Prédisposition génétique à une maladie</term>
<term>Valeur prédictive des tests</term>
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<front><div type="abstract" xml:lang="en">Milroy disease is a congenital onset lymphedema linked to FLT4 gene mutations in the tyrosine kinase domain. So far, a total of 59 different FLT4 variants have been identified. Here, we report a novel FLT4 gene mutation in a Chinese family with Milroy disease and present their clinical symptoms and MR lymphangiographic findings.</div>
</front>
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<Issue>2</Issue>
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<Title>Lymphology</Title>
<ISOAbbreviation>Lymphology</ISOAbbreviation>
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<ArticleTitle>A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE.</ArticleTitle>
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<Abstract><AbstractText>Milroy disease is a congenital onset lymphedema linked to FLT4 gene mutations in the tyrosine kinase domain. So far, a total of 59 different FLT4 variants have been identified. Here, we report a novel FLT4 gene mutation in a Chinese family with Milroy disease and present their clinical symptoms and MR lymphangiographic findings.</AbstractText>
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A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE.

A NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE.

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)

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Pour générer des pages wiki