Clinical and familial studies in the Noonan syndrome.
Identifieur interne : 010616 ( Main/Exploration ); précédent : 010615; suivant : 010617Clinical and familial studies in the Noonan syndrome.
Auteurs : V B Penchaszadeh ; R. Coco ; R. Farías ; C. BergadáSource :
- Birth defects original article series [ 0547-6844 ] ; 1974.
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:
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Le document en format XML
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</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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<author><name sortKey="Coco, R" sort="Coco, R" uniqKey="Coco R" first="R" last="Coco">R. Coco</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>
</keywords>
<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>
</keywords>
<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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