首页> 外文期刊>The journal of maternal-fetal & neonatal medicine >Turner's syndrome and pregnancy: has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review.
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Turner's syndrome and pregnancy: has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review.

机译:特纳综合征和妊娠:45,X / 47,XXX镶嵌症是否有不同的预后?自己的临床经验和文献回顾。

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摘要

Turner's syndrome is characterized by an ovarian failure which occurs in most cases before puberty and leads to infertility. In less than 10% of women with Turner syndrome, puberty may occur and spontaneous pregnancies is possible but with a high risk of fetal loss, chromosomal and congenital abnormalities. We present the case of a 33-year-old woman with a mosaic Turner's syndrome karyotype 45,X/47,XXX who conceived spontaneously and had two successful pregnancies. Short stature was the only manifestation of Turner's syndrome. In the present report, we reviewed the available literature on the fertility of women with Turner's syndrome and the phenotypic effects of mosaicism for a 47,XXX cell line in Turner's syndrome.
机译:特纳综合症的特征是卵巢衰竭,多数情况下发生在青春期之前,并导致不孕。在不到10%的特纳综合征女性中,可能发生青春期并可能自发怀孕,但胎儿丢失,染色体和先天性异常的风险很高。我们介绍了一个33岁的女性,患有马赛克特纳氏综合症的染色体核型45,X / 47,XXX,该患者自发受孕并两次成功怀孕。身材矮小是特纳氏综合症的唯一表现。在本报告中,我们回顾了有关特纳氏综合症妇女的生育能力以及特纳氏综合症中47,XXX细胞系镶嵌症的表型效应的现有文献。

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