[Congenital soft tissue dysplasia. A new anatomo-clinical entity].
Identifieur interne : 00ED09 ( Main/Exploration ); précédent : 00ED08; suivant : 00ED10[Congenital soft tissue dysplasia. A new anatomo-clinical entity].
Auteurs : D. Pellerin ; H. Martelli ; X. Latouche ; F. GasnierSource :
- Chirurgie; memoires de l'Academie de chirurgie [ 0001-4001 ] ; 1985.
Descripteurs français
- KwdFr :
- Ectoderme (anatomopathologie), Enfant, Enfant d'âge préscolaire, Femelle, Gigantisme (anatomopathologie), Hamartomes (anatomopathologie), Humains, Lymphoedème (), Malformations multiples (), Malformations multiples (anatomopathologie), Mâle, Mésoderme (anatomopathologie), Neurofibromatose de type 1 (anatomopathologie), Nourrisson, Nouveau-né, Syndrome de Klippel-Trénaunay (anatomopathologie), Tumeurs des tissus mous (anatomopathologie).
- MESH :
English descriptors
- KwdEn :
- Abnormalities, Multiple (pathology), Abnormalities, Multiple (therapy), Child, Child, Preschool, Ectoderm (pathology), Female, Gigantism (pathology), Hamartoma (pathology), Humans, Infant, Infant, Newborn, Klippel-Trenaunay-Weber Syndrome (pathology), Lymphedema (congenital), Male, Mesoderm (pathology), Neurofibromatosis 1 (pathology), Soft Tissue Neoplasms (pathology).
- MESH :
- congenital : Lymphedema.
- pathology : Abnormalities, Multiple, Ectoderm, Gigantism, Hamartoma, Klippel-Trenaunay-Weber Syndrome, Mesoderm, Neurofibromatosis 1, Soft Tissue Neoplasms.
- therapy : Abnormalities, Multiple.
- Child, Child, Preschool, Female, Humans, Infant, Infant, Newborn, Male.
PubMed: 3013512
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 006882
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- to stream PubMed, to step Checkpoint: 006882
- to stream Ncbi, to step Merge: 009521
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- to stream Main, to step Merge: 00FA90
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Le document en format XML
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<author><name sortKey="Martelli, H" sort="Martelli, H" uniqKey="Martelli H" first="H" last="Martelli">H. Martelli</name>
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<author><name sortKey="Latouche, X" sort="Latouche, X" uniqKey="Latouche X" first="X" last="Latouche">X. Latouche</name>
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<series><title level="j">Chirurgie; memoires de l'Academie de chirurgie</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Abnormalities, Multiple (pathology)</term>
<term>Abnormalities, Multiple (therapy)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Ectoderm (pathology)</term>
<term>Female</term>
<term>Gigantism (pathology)</term>
<term>Hamartoma (pathology)</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Klippel-Trenaunay-Weber Syndrome (pathology)</term>
<term>Lymphedema (congenital)</term>
<term>Male</term>
<term>Mesoderm (pathology)</term>
<term>Neurofibromatosis 1 (pathology)</term>
<term>Soft Tissue Neoplasms (pathology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Ectoderme (anatomopathologie)</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Gigantisme (anatomopathologie)</term>
<term>Hamartomes (anatomopathologie)</term>
<term>Humains</term>
<term>Lymphoedème ()</term>
<term>Malformations multiples ()</term>
<term>Malformations multiples (anatomopathologie)</term>
<term>Mâle</term>
<term>Mésoderme (anatomopathologie)</term>
<term>Neurofibromatose de type 1 (anatomopathologie)</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
<term>Syndrome de Klippel-Trénaunay (anatomopathologie)</term>
<term>Tumeurs des tissus mous (anatomopathologie)</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Ectoderme</term>
<term>Gigantisme</term>
<term>Hamartomes</term>
<term>Malformations multiples</term>
<term>Mésoderme</term>
<term>Neurofibromatose de type 1</term>
<term>Syndrome de Klippel-Trénaunay</term>
<term>Tumeurs des tissus mous</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Abnormalities, Multiple</term>
<term>Ectoderm</term>
<term>Gigantism</term>
<term>Hamartoma</term>
<term>Klippel-Trenaunay-Weber Syndrome</term>
<term>Mesoderm</term>
<term>Neurofibromatosis 1</term>
<term>Soft Tissue Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Abnormalities, Multiple</term>
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<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Infant</term>
<term>Infant, Newborn</term>
<term>Male</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphoedème</term>
<term>Malformations multiples</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Nouveau-né</term>
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<name sortKey="Latouche, X" sort="Latouche, X" uniqKey="Latouche X" first="X" last="Latouche">X. Latouche</name>
<name sortKey="Martelli, H" sort="Martelli, H" uniqKey="Martelli H" first="H" last="Martelli">H. Martelli</name>
<name sortKey="Pellerin, D" sort="Pellerin, D" uniqKey="Pellerin D" first="D" last="Pellerin">D. Pellerin</name>
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