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Is the prevalence of Klinefelter syndrome increasing?

机译:Klinefelter综合征的患病率增加了吗?

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The birth prevalence of sex chromosome trisomies (SCT), that is individuals with an XYY, XXY or XXX sex chromosome constitution, is traditionally based on six surveys of unselected newborns carried out in the 1960s and early 1970s. All three SCTs had a prevalence of 1 in 1000 same sex births. We re-examined these prevalences based on additional cytogenetic studies of newborn surveys, spontaneous abortions, perinatal deaths and prenatal diagnoses. The more recent newborn surveys suggest there has been an increase in the prevalence of XXYs, but not of the other two SCTs since the original newborn series. The prevalence of XXYs has risen from 1.09 to 1.72 per 1000 male births (P=0.023). We suggest that such an increase, in the absence of an increase in the prevalence of XXX, is unlikely to be due to increased maternal age. As XXY is the only chromosome abnormality known where a substantial proportion ( approximately 50%) arise as the result of non-disjunction at the first paternal meiotic division, we speculate that some factor may be interfering with pairing and/or recombination of the sex bivalent at the paternal MI division.European Journal of Human Genetics (2008) 16, 163-170; doi:10.1038/sj.ejhg.5201956; published online 14 November 2007.
机译:传统上,性染色体三体性(SCT)(即具有XYY,XXY或XXX性染色体组成的个体)的出生率传统上是基于对1960年代和1970年代初进行的六项未选新生儿的调查。所有三个SCT的患病率均为1000个同性出生中的1个。我们根据对新生儿调查,自然流产,围产儿死亡和产前诊断的其他细胞遗传学研究,重新检查了这些患病率。最近的新生儿调查表明,自原始新生儿系列以来,XXY的患病率有所增加,但其他两个SCT的患病率却没有增加。每1000例男性出生的XXY患病率从1.09上升到1.72(P = 0.023)。我们建议,在没有XXX患病率增加的情况下,这种增加不太可能是由于产妇年龄的增加。由于XXY是已知的唯一染色体异常,其中第一次父系减数分裂时不分离导致显着比例的染色体异常(大约50%),因此我们推测某些因素可能会干扰二价性的配对和/或重组欧洲父本遗传学杂志(2008)16,163-170; doi:10.1038 / sj.ejhg.5201956;在线发布于2007年11月14日。

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