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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.
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页码:359 / 367
页数:9
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