The female and the fragile X reviewed

被引:13
作者
Kenneson, A
Warren, ST
机构
[1] Emory Univ, Sch Med, Dept Biochem Genet & Pediat, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Hughes Med Inst, Atlanta, GA 30322 USA
关键词
fragile X syndrome; FMR1; FMRP; premature ovarian failure; trinucleotide repeat;
D O I
10.1055/s-2001-15401
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Nearly 15 years ago, female carriers of the fragile X mental retardation syndrome were noted to have an increased incidence of tu in pregnancies. Since then, much evidence has accumulated supporting the notion of ovarian dysfunction in fragile X carriers, in the forms of increased dizygotic twinning and premature ovarian failure. However, despite a decade and a half of research regarding this association, the underlying mechanism remains a mystery. This article reviews the population-based studies that have examined this association and discusses possible reasons for the variations in results. In addition, results from more recent studies on endocrine function in fragile X carriers are discussed. These data, when considered in conjunction with our emerging understanding of the molecular biology of the fragile X gene (FMR1) and its protein product (FMRP), are beginning to elucidate possible mechanisms for the association between fragile X syndrome and ovarian dysfunction.
引用
收藏
页码:159 / 165
页数:7
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