Turner's syndrome and mosaicism

被引:5
|
作者
Battin, J [1 ]
机构
[1] CHU Pellegrin, Hop Enfants, Serv Genet Med, F-33076 Bordeaux, France
来源
BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE | 2003年 / 187卷 / 02期
关键词
Turner syndrome; mosaicism; X chromosome; phenotype; genotype; twins; monozygotics; genetics;
D O I
10.1016/S0001-4079(19)34055-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Turner's syndrome is a gonadosomatic dysgenesis of female phenotype due to a more or less complete monosomy of one of the X chromosomes leading to a hoploinsufficiency of the development genes situated at the level of the pseudoautosomal region of the gonosomes. Further experience of the karyotype showed a preponderance of mosaics and considerable variability of Turner's phenotype in proportion to the number of 45, X cells. The rare cases of monozygotism discordant with variable tissular distribution mosaics show that the phenotypic expression is a genic dosage effect. In patients with TS it would thus be of interest to study a second tissue such skin fibroblasts when a discordance is observed between the phenotype and the karyotype.
引用
收藏
页码:359 / 367
页数:9
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