A Chinese pedigree of lymphoedema-distichiasis syndrome with a novel mutation in the FOXC2 gene.
Identifieur interne : 002E70 ( Main/Exploration ); précédent : 002E69; suivant : 002E71A Chinese pedigree of lymphoedema-distichiasis syndrome with a novel mutation in the FOXC2 gene.
Auteurs : L-L Zhu [République populaire de Chine] ; Y-N Lv ; H-D Chen ; X-H GaoSource :
- Clinical and experimental dermatology [ 1365-2230 ] ; 2014.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Facteurs de transcription Forkhead, Lymphoedème.
- malformations : Cils.
- Adolescent, Humains, Mutation faux-sens, Mâle, Pedigree.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Forkhead Transcription Factors.
- abnormalities : Eyelashes.
- genetics : Lymphedema.
- Adolescent, Humans, Male, Mutation, Missense, Pedigree.
Abstract
Lymphoedema-distichiasis syndrome (LDS) is a syndromic form of primary lymphoedema associated with double rows of eyelashes (distichiasis). Mutations in the FOXC2 gene were reported to be associated with this syndrome. In this study, we identified in a Chinese LDS pedigree a novel FOXC2 gene mutation, C.370C>T, leading to p.Leu124Phe. The novel mutation is not a common polymorphism, but is co-inherited with the disease.
DOI: 10.1111/ced.12389
PubMed: 24984567
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 001459
- to stream PubMed, to step Curation: 001459
- to stream PubMed, to step Checkpoint: 001459
- to stream Ncbi, to step Merge: 006810
- to stream Ncbi, to step Curation: 006810
- to stream Ncbi, to step Checkpoint: 006810
- to stream Main, to step Merge: 002E75
- to stream Main, to step Curation: 002E70
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">A Chinese pedigree of lymphoedema-distichiasis syndrome with a novel mutation in the FOXC2 gene.</title>
<author><name sortKey="Zhu, L L" sort="Zhu, L L" uniqKey="Zhu L" first="L-L" last="Zhu">L-L Zhu</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Dermatology, No.1 Hospital of China Medical University, China; Department of Dermatology, The People's Hospital of Liaoning Province, China.</nlm:affiliation>
<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>Department of Dermatology, No.1 Hospital of China Medical University, China; Department of Dermatology, The People's Hospital of Liaoning Province</wicri:regionArea>
<wicri:noRegion>The People's Hospital of Liaoning Province</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Lv, Y N" sort="Lv, Y N" uniqKey="Lv Y" first="Y-N" last="Lv">Y-N Lv</name>
</author>
<author><name sortKey="Chen, H D" sort="Chen, H D" uniqKey="Chen H" first="H-D" last="Chen">H-D Chen</name>
</author>
<author><name sortKey="Gao, X H" sort="Gao, X H" uniqKey="Gao X" first="X-H" last="Gao">X-H Gao</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2014">2014</date>
<idno type="RBID">pubmed:24984567</idno>
<idno type="pmid">24984567</idno>
<idno type="doi">10.1111/ced.12389</idno>
<idno type="wicri:Area/PubMed/Corpus">001459</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">001459</idno>
<idno type="wicri:Area/PubMed/Curation">001459</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">001459</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001459</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">001459</idno>
<idno type="wicri:Area/Ncbi/Merge">006810</idno>
<idno type="wicri:Area/Ncbi/Curation">006810</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">006810</idno>
<idno type="wicri:Area/Main/Merge">002E75</idno>
<idno type="wicri:Area/Main/Curation">002E70</idno>
<idno type="wicri:Area/Main/Exploration">002E70</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">A Chinese pedigree of lymphoedema-distichiasis syndrome with a novel mutation in the FOXC2 gene.</title>
<author><name sortKey="Zhu, L L" sort="Zhu, L L" uniqKey="Zhu L" first="L-L" last="Zhu">L-L Zhu</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Dermatology, No.1 Hospital of China Medical University, China; Department of Dermatology, The People's Hospital of Liaoning Province, China.</nlm:affiliation>
<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>Department of Dermatology, No.1 Hospital of China Medical University, China; Department of Dermatology, The People's Hospital of Liaoning Province</wicri:regionArea>
<wicri:noRegion>The People's Hospital of Liaoning Province</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Lv, Y N" sort="Lv, Y N" uniqKey="Lv Y" first="Y-N" last="Lv">Y-N Lv</name>
</author>
<author><name sortKey="Chen, H D" sort="Chen, H D" uniqKey="Chen H" first="H-D" last="Chen">H-D Chen</name>
</author>
<author><name sortKey="Gao, X H" sort="Gao, X H" uniqKey="Gao X" first="X-H" last="Gao">X-H Gao</name>
</author>
</analytic>
<series><title level="j">Clinical and experimental dermatology</title>
<idno type="eISSN">1365-2230</idno>
<imprint><date when="2014" type="published">2014</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Eyelashes (abnormalities)</term>
<term>Forkhead Transcription Factors (genetics)</term>
<term>Humans</term>
<term>Lymphedema (genetics)</term>
<term>Male</term>
<term>Mutation, Missense</term>
<term>Pedigree</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term>
<term>Cils (malformations)</term>
<term>Facteurs de transcription Forkhead (génétique)</term>
<term>Humains</term>
<term>Lymphoedème (génétique)</term>
<term>Mutation faux-sens</term>
<term>Mâle</term>
<term>Pedigree</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Forkhead Transcription Factors</term>
</keywords>
<keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Eyelashes</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Facteurs de transcription Forkhead</term>
<term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" qualifier="malformations" xml:lang="fr"><term>Cils</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Humans</term>
<term>Male</term>
<term>Mutation, Missense</term>
<term>Pedigree</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Humains</term>
<term>Mutation faux-sens</term>
<term>Mâle</term>
<term>Pedigree</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Lymphoedema-distichiasis syndrome (LDS) is a syndromic form of primary lymphoedema associated with double rows of eyelashes (distichiasis). Mutations in the FOXC2 gene were reported to be associated with this syndrome. In this study, we identified in a Chinese LDS pedigree a novel FOXC2 gene mutation, C.370C>T, leading to p.Leu124Phe. The novel mutation is not a common polymorphism, but is co-inherited with the disease.</div>
</front>
</TEI>
<affiliations><list><country><li>République populaire de Chine</li>
</country>
</list>
<tree><noCountry><name sortKey="Chen, H D" sort="Chen, H D" uniqKey="Chen H" first="H-D" last="Chen">H-D Chen</name>
<name sortKey="Gao, X H" sort="Gao, X H" uniqKey="Gao X" first="X-H" last="Gao">X-H Gao</name>
<name sortKey="Lv, Y N" sort="Lv, Y N" uniqKey="Lv Y" first="Y-N" last="Lv">Y-N Lv</name>
</noCountry>
<country name="République populaire de Chine"><noRegion><name sortKey="Zhu, L L" sort="Zhu, L L" uniqKey="Zhu L" first="L-L" last="Zhu">L-L Zhu</name>
</noRegion>
</country>
</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 002E70 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002E70 | 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= pubmed:24984567 |texte= A Chinese pedigree of lymphoedema-distichiasis syndrome with a novel mutation in the FOXC2 gene. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:24984567" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \ | NlmPubMed2Wicri -a LymphedemaV1
![]() | This area was generated with Dilib version V0.6.31. | ![]() |