LymphedemaV1, Main, Exploration, bibRecord, 010616

Clinical and familial studies in the Noonan syndrome.

Identifieur interne : 010616 ( Main/Exploration ); précédent : 010615; suivant : 010617

Clinical and familial studies in the Noonan syndrome.

Auteurs : V B Penchaszadeh ; R. Coco ; R. Farías ; C. Bergadá

Source :

Birth defects original article series [ 0547-6844 ] ; 1974.

RBID : pubmed:4376701

Descripteurs français

KwdFr :
- Adolescent, Adulte, Cou, Coude (malformations), Dermatoglyphes, Déficience intellectuelle (épidémiologie), Détermination de l'âge osseux, Enfant, Enfant d'âge préscolaire, Femelle, Humains, Hydronéphrose (épidémiologie), Lymphoedème (), Main, Malformations cardiovasculaires, Malformations oculaires, Micrognathisme (épidémiologie), Mâle, Nanisme (épidémiologie), Oreille, Parents, Pedigree, Phénotype, Syndrome, Syndrome de Turner (diagnostic), Syndrome de Turner (génétique), Âge maternel.
MESH :
- diagnostic : Syndrome de Turner.
- génétique : Syndrome de Turner.
- malformations : Coude.
- épidémiologie : Déficience intellectuelle, Hydronéphrose, Micrognathisme, Nanisme.
- Adolescent, Adulte, Cou, Dermatoglyphes, Détermination de l'âge osseux, Enfant, Enfant d'âge préscolaire, Femelle, Humains, Lymphoedème, Main, Malformations cardiovasculaires, Malformations oculaires, Mâle, Oreille, Parents, Pedigree, Phénotype, Syndrome, Âge maternel.

English descriptors

KwdEn :
- Adolescent, Adult, Age Determination by Skeleton, Cardiovascular Abnormalities, Child, Child, Preschool, Dermatoglyphics, Dwarfism (epidemiology), Ear, Elbow (abnormalities), Eye Abnormalities, Female, Hand, Humans, Hydronephrosis (epidemiology), Intellectual Disability (epidemiology), Lymphedema (congenital), Male, Maternal Age, Micrognathism (epidemiology), Neck, Parents, Pedigree, Phenotype, Syndrome, Turner Syndrome (diagnosis), Turner Syndrome (genetics).
MESH :
- abnormalities : Elbow.
- congenital : Lymphedema.
- diagnosis : Turner Syndrome.
- epidemiology : Dwarfism, Hydronephrosis, Intellectual Disability, Micrognathism.
- genetics : Turner Syndrome.
- Adolescent, Adult, Age Determination by Skeleton, Cardiovascular Abnormalities, Child, Child, Preschool, Dermatoglyphics, Ear, Eye Abnormalities, Female, Hand, Humans, Male, Maternal Age, Neck, Parents, Pedigree, Phenotype, Syndrome.

PubMed: 4376701

Affiliations:

Le document en format XML

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<author><name sortKey="Penchaszadeh, V B" sort="Penchaszadeh, V B" uniqKey="Penchaszadeh V" first="V B" last="Penchaszadeh">V B Penchaszadeh</name>
</author>
<author><name sortKey="Coco, R" sort="Coco, R" uniqKey="Coco R" first="R" last="Coco">R. Coco</name>
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<author><name sortKey="Farias, R" sort="Farias, R" uniqKey="Farias R" first="R" last="Farías">R. Farías</name>
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<author><name sortKey="Bergada, C" sort="Bergada, C" uniqKey="Bergada C" first="C" last="Bergadá">C. Bergadá</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Age Determination by Skeleton</term>
<term>Cardiovascular Abnormalities</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Dermatoglyphics</term>
<term>Dwarfism (epidemiology)</term>
<term>Ear</term>
<term>Elbow (abnormalities)</term>
<term>Eye Abnormalities</term>
<term>Female</term>
<term>Hand</term>
<term>Humans</term>
<term>Hydronephrosis (epidemiology)</term>
<term>Intellectual Disability (epidemiology)</term>
<term>Lymphedema (congenital)</term>
<term>Male</term>
<term>Maternal Age</term>
<term>Micrognathism (epidemiology)</term>
<term>Neck</term>
<term>Parents</term>
<term>Pedigree</term>
<term>Phenotype</term>
<term>Syndrome</term>
<term>Turner Syndrome (diagnosis)</term>
<term>Turner Syndrome (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Adolescent</term>
<term>Adulte</term>
<term>Cou</term>
<term>Coude (malformations)</term>
<term>Dermatoglyphes</term>
<term>Déficience intellectuelle (épidémiologie)</term>
<term>Détermination de l'âge osseux</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Hydronéphrose (épidémiologie)</term>
<term>Lymphoedème ()</term>
<term>Main</term>
<term>Malformations cardiovasculaires</term>
<term>Malformations oculaires</term>
<term>Micrognathisme (épidémiologie)</term>
<term>Mâle</term>
<term>Nanisme (épidémiologie)</term>
<term>Oreille</term>
<term>Parents</term>
<term>Pedigree</term>
<term>Phénotype</term>
<term>Syndrome</term>
<term>Syndrome de Turner (diagnostic)</term>
<term>Syndrome de Turner (génétique)</term>
<term>Âge maternel</term>
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<keywords scheme="MESH" qualifier="abnormalities" xml:lang="en"><term>Elbow</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Turner Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Syndrome de Turner</term>
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<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Dwarfism</term>
<term>Hydronephrosis</term>
<term>Intellectual Disability</term>
<term>Micrognathism</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Turner Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Syndrome de Turner</term>
</keywords>
<keywords scheme="MESH" qualifier="malformations" xml:lang="fr"><term>Coude</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr"><term>Déficience intellectuelle</term>
<term>Hydronéphrose</term>
<term>Micrognathisme</term>
<term>Nanisme</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Adult</term>
<term>Age Determination by Skeleton</term>
<term>Cardiovascular Abnormalities</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Dermatoglyphics</term>
<term>Ear</term>
<term>Eye Abnormalities</term>
<term>Female</term>
<term>Hand</term>
<term>Humans</term>
<term>Male</term>
<term>Maternal Age</term>
<term>Neck</term>
<term>Parents</term>
<term>Pedigree</term>
<term>Phenotype</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Adolescent</term>
<term>Adulte</term>
<term>Cou</term>
<term>Dermatoglyphes</term>
<term>Détermination de l'âge osseux</term>
<term>Enfant</term>
<term>Enfant d'âge préscolaire</term>
<term>Femelle</term>
<term>Humains</term>
<term>Lymphoedème</term>
<term>Main</term>
<term>Malformations cardiovasculaires</term>
<term>Malformations oculaires</term>
<term>Mâle</term>
<term>Oreille</term>
<term>Parents</term>
<term>Pedigree</term>
<term>Phénotype</term>
<term>Syndrome</term>
<term>Âge maternel</term>
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<tree><noCountry><name sortKey="Bergada, C" sort="Bergada, C" uniqKey="Bergada C" first="C" last="Bergadá">C. Bergadá</name>
<name sortKey="Coco, R" sort="Coco, R" uniqKey="Coco R" first="R" last="Coco">R. Coco</name>
<name sortKey="Farias, R" sort="Farias, R" uniqKey="Farias R" first="R" last="Farías">R. Farías</name>
<name sortKey="Penchaszadeh, V B" sort="Penchaszadeh, V B" uniqKey="Penchaszadeh V" first="V B" last="Penchaszadeh">V B Penchaszadeh</name>
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Serveur d'exploration sur le lymphœdème

Clinical and familial studies in the Noonan syndrome.

Clinical and familial studies in the Noonan syndrome.

Source :

Descripteurs français

English descriptors

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki

	Serveur d'exploration sur le lymphœdème
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