[Meige-Milroy-Nonne disease. Report of a case in a six-month-old infant].
Identifieur interne : 00D918 ( Main/Exploration ); précédent : 00D917; suivant : 00D919[Meige-Milroy-Nonne disease. Report of a case in a six-month-old infant].
Auteurs : N. Kubryk ; M. RogerSource :
- Annales de pediatrie [ 0066-2097 ] ; 1990.
Descripteurs français
- KwdFr :
- MESH :
- diagnostic : Lymphoedème.
- génétique : Lymphoedème.
- Diagnostic différentiel, Humains, Lymphoedème, Mâle, Nourrisson, Pedigree.
English descriptors
- KwdEn :
- MESH :
- congenital : Lymphedema.
- diagnosis : Lymphedema.
- genetics : Lymphedema.
- Diagnosis, Differential, Humans, Infant, Male, Pedigree.
Abstract
A case of Milroy disease is reported. This very infrequent condition is a familial disease characterized by the presence of lymphedema of the lower limbs. In our patient's family, we identified 12 affected members belonging to four generations.
PubMed: 2256646
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 005D06
- to stream PubMed, to step Curation: 005D06
- to stream PubMed, to step Checkpoint: 005D06
- to stream Ncbi, to step Merge: 004D48
- to stream Ncbi, to step Curation: 004D48
- to stream Ncbi, to step Checkpoint: 004D48
- to stream Main, to step Merge: 00E486
- to stream Main, to step Curation: 00D918
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">[Meige-Milroy-Nonne disease. Report of a case in a six-month-old infant].</title>
<author><name sortKey="Kubryk, N" sort="Kubryk, N" uniqKey="Kubryk N" first="N" last="Kubryk">N. Kubryk</name>
<affiliation><nlm:affiliation>Centre pédiatrique Saint-Lambert, Lioux, Gordes.</nlm:affiliation>
<wicri:noCountry code="subField">Gordes</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Roger, M" sort="Roger, M" uniqKey="Roger M" first="M" last="Roger">M. Roger</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1990">1990</date>
<idno type="RBID">pubmed:2256646</idno>
<idno type="pmid">2256646</idno>
<idno type="wicri:Area/PubMed/Corpus">005D06</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">005D06</idno>
<idno type="wicri:Area/PubMed/Curation">005D06</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">005D06</idno>
<idno type="wicri:Area/PubMed/Checkpoint">005D06</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">005D06</idno>
<idno type="wicri:Area/Ncbi/Merge">004D48</idno>
<idno type="wicri:Area/Ncbi/Curation">004D48</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">004D48</idno>
<idno type="wicri:doubleKey">0066-2097:1990:Kubryk N:meige:milroy:nonne</idno>
<idno type="wicri:Area/Main/Merge">00E486</idno>
<idno type="wicri:Area/Main/Curation">00D918</idno>
<idno type="wicri:Area/Main/Exploration">00D918</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">[Meige-Milroy-Nonne disease. Report of a case in a six-month-old infant].</title>
<author><name sortKey="Kubryk, N" sort="Kubryk, N" uniqKey="Kubryk N" first="N" last="Kubryk">N. Kubryk</name>
<affiliation><nlm:affiliation>Centre pédiatrique Saint-Lambert, Lioux, Gordes.</nlm:affiliation>
<wicri:noCountry code="subField">Gordes</wicri:noCountry>
</affiliation>
</author>
<author><name sortKey="Roger, M" sort="Roger, M" uniqKey="Roger M" first="M" last="Roger">M. Roger</name>
</author>
</analytic>
<series><title level="j">Annales de pediatrie</title>
<idno type="ISSN">0066-2097</idno>
<imprint><date when="1990" type="published">1990</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Diagnosis, Differential</term>
<term>Humans</term>
<term>Infant</term>
<term>Lymphedema (congenital)</term>
<term>Lymphedema (diagnosis)</term>
<term>Lymphedema (genetics)</term>
<term>Male</term>
<term>Pedigree</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Diagnostic différentiel</term>
<term>Humains</term>
<term>Lymphoedème ()</term>
<term>Lymphoedème (diagnostic)</term>
<term>Lymphoedème (génétique)</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Pedigree</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Diagnosis, Differential</term>
<term>Humans</term>
<term>Infant</term>
<term>Male</term>
<term>Pedigree</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Diagnostic différentiel</term>
<term>Humains</term>
<term>Lymphoedème</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Pedigree</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">A case of Milroy disease is reported. This very infrequent condition is a familial disease characterized by the presence of lymphedema of the lower limbs. In our patient's family, we identified 12 affected members belonging to four generations.</div>
</front>
</TEI>
<affiliations><list></list>
<tree><noCountry><name sortKey="Kubryk, N" sort="Kubryk, N" uniqKey="Kubryk N" first="N" last="Kubryk">N. Kubryk</name>
<name sortKey="Roger, M" sort="Roger, M" uniqKey="Roger M" first="M" last="Roger">M. Roger</name>
</noCountry>
</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 00D918 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 00D918 | 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:2256646 |texte= [Meige-Milroy-Nonne disease. Report of a case in a six-month-old infant]. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:2256646" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \ | NlmPubMed2Wicri -a LymphedemaV1
![]() | This area was generated with Dilib version V0.6.31. | ![]() |