LymphedemaV1, Main, Exploration, bibRecordById, pubmed:4164063

CHROMOSOME ANOMALIES IN PRIMARY LYMPHŒDEMA

Identifieur interne : 011173 ( Main/Exploration ); précédent : 011172; suivant : 011174

CHROMOSOME ANOMALIES IN PRIMARY LYMPHŒDEMA

Auteurs : Philipf. Benson [Royaume-Uni] ; Angelai. Taylor [Royaume-Uni] ; Malcolmh. Gough [Royaume-Uni]

Source :

The Lancet [ 0140-6736 ] ; 1967.

RBID : ISTEX:83649748F17E25A0C8FD6D173737EEE7FFE500D0

Descripteurs français

KwdFr :
- Aberrations des chromosomes (épidémiologie), Adolescent, Adulte, Adulte d'âge moyen, Cartographie chromosomique, Enfant, Enfant d'âge préscolaire, Femelle, Humains, Lymphoedème (), Lymphographie, Maladies chromosomiques, Mâle, Sujet âgé.
MESH :
- épidémiologie : Aberrations des chromosomes.
- Adolescent, Adulte, Adulte d'âge moyen, Cartographie chromosomique, Enfant, Enfant d'âge préscolaire, Femelle, Humains, Lymphoedème, Lymphographie, Maladies chromosomiques, Mâle, Sujet âgé.

English descriptors

KwdEn :
- Adolescent, Adult, Aged, Child, Child, Preschool, Chromosome Aberrations (epidemiology), Chromosome Disorders, Chromosome Mapping, Female, Humans, Lymphedema (complications), Lymphography, Male, Middle Aged.
MESH :
- complications : Lymphedema.
- epidemiology : Chromosome Aberrations.
- Adolescent, Adult, Aged, Child, Child, Preschool, Chromosome Disorders, Chromosome Mapping, Female, Humans, Lymphography, Male, Middle Aged.

Abstract

37 unselected patients with primary lymphœdema were investigated. Of 32 phenotypic females, 26 had normal karyotypes; 2 had an XO sex-chromosome complement; 1 had probable XO/XX mosaicism; 2 had an XY sex-chromosome complement; and 1 had a ring chromosome replacing one of the " G " group autosomes in 4% of leucocytes—an anomaly which has not been reported previously. All 5 males had normal karyotypes. Chromosome studies should be considered in patients with primary lymphœdema, especially if it is congenital and subsequently disappears, or if there are associated features of ovarian dysgenesis.

Url:

https://api.istex.fr/document/83649748F17E25A0C8FD6D173737EEE7FFE500D0/fulltext/pdf

DOI: 10.1016/S0140-6736(67)91088-4

Affiliations:

Le document en format XML

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<term>Chromosome Aberrations (epidemiology)</term>
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<term>Chromosome Mapping</term>
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<term>Enfant d'âge préscolaire</term>
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<term>Lymphoedème ()</term>
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<term>Maladies chromosomiques</term>
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<front><div type="abstract" xml:lang="en">37 unselected patients with primary lymphœdema were investigated. Of 32 phenotypic females, 26 had normal karyotypes; 2 had an XO sex-chromosome complement; 1 had probable XO/XX mosaicism; 2 had an XY sex-chromosome complement; and 1 had a ring chromosome replacing one of the " G " group autosomes in 4% of leucocytes—an anomaly which has not been reported previously. All 5 males had normal karyotypes. Chromosome studies should be considered in patients with primary lymphœdema, especially if it is congenital and subsequently disappears, or if there are associated features of ovarian dysgenesis.</div>
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Serveur d'exploration sur le lymphœdème

CHROMOSOME ANOMALIES IN PRIMARY LYMPHŒDEMA

CHROMOSOME ANOMALIES IN PRIMARY LYMPHŒDEMA

Source :

Descripteurs français

English descriptors

Abstract

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

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Pour manipuler ce document sous Unix (Dilib)

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