Genetic analysis of mosaicism in 53 women with Turner syndrome

被引:45
作者
Hanson, L [1 ]
Bryman, I
Barrenäs, ML
Janson, PO
Wahlström, J
Albertsson-Wikland, K
Hanson, C
机构
[1] Gothenburg Univ, Sahlgrenska Hosp, Dept Obstet & Gynecol, SE-41345 Gothenburg, Sweden
[2] Gothenburg Univ, Sahlgrenska Hosp, Dept Pediat, Gothenburg Pediat Growth Res Ctr, SE-41345 Gothenburg, Sweden
[3] Gothenburg Univ, Sahlgrenska Hosp, Dept Clin Genet, SE-41345 Gothenburg, Sweden
关键词
D O I
10.1111/j.1601-5223.2001.00153.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mosaicism involving the sex chromosomes is a common finding in women with Turner syndrome (TS). It is especially important to detect Y-chromosomal material, since this is a risk factor for the development of gonadoblastoma. Recent studies have also indicated that the frequency of 45,X cells may be used to predict prognosis. As part of an ongoing multi-disciplinary study, we have examined the extent of Y-chromosomal material and sex chromosomal mosaicism and its tissue specificity in 53 women with TS. The results of lymphocyte karyotyping were compared with the use of interphase X/Y fluorescence in situ hybridisation (FISH) analysis of lymphocytes and buccal mucosal cells. As could be expected, an extended FISH analysis detected more Y-chromosomal material than karyotyping (in 15 % vs. 11 % of the women, respectively) and also detected more X-chromosomal mosaicism among the TS women (in 70 % vs. 45 % of the women, respectively). In half of the women, tissue-specific differences between lymphocytes and buccal mucosal cells were found. Based on these results, we suggest the use of X/Y interphase FISH as a complement to karyotyping in order to obtain a more complete knowledge of the chromosome constitution of each individual with TS.
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页码:153 / 159
页数:7
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