CHROMOSOME ANOMALIES IN PRIMARY LYMPHŒDEMA
Identifieur interne : 003D99 ( Istex/Curation ); précédent : 003D98; suivant : 003E00CHROMOSOME ANOMALIES IN PRIMARY LYMPHŒDEMA
Auteurs : Philipf. Benson [Royaume-Uni] ; Angelai. Taylor [Royaume-Uni] ; Malcolmh. Gough [Royaume-Uni]Source :
- The Lancet [ 0140-6736 ] ; 1967.
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.
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DOI: 10.1016/S0140-6736(67)91088-4
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