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根据人工流产和自然流产数据估算人类妊娠中染色体数目异常的发生率。

Incidence of numerical chromosome anomalies in human pregnancy estimation from induced and spontaneous abortion data.

作者信息

Burgoyne P S, Holland K, Stephens R

机构信息

MRC Mammalian Development Unit, London, UK.

出版信息

Hum Reprod. 1991 Apr;6(4):555-65. doi: 10.1093/oxfordjournals.humrep.a137379.

Abstract

Induced abortion data provided an estimate of 4.7% numerical chromosome anomalies for women with a clinically recognized pregnancy at the end of the 7th week after the last menstrual period (LMP). This frequency requires that 51.9% of spontaneous abortions occurring after the 7th week should be chromosomally abnormal if the frequency of numerical chromosome anomalies at term (live and stillbirths combined) is 0.53%. Cytogenetic data from surveys of spontaneous abortion suggested a lower incidence of 39.7%. However, this figure is likely to be an underestimate because chromosome anomalies are almost certainly over-represented among the many early abortuses which lack embryonic tissue and hence are not karyotyped. The frequency of numerical chromosome anomalies at conception, arising from meiotic errors, was estimated from sperm karyotype data combined with information on the relative frequencies of maternal and paternal errors in the aetiology of trisomies. This provided a minimum estimate of 20%.

摘要

人工流产数据显示,末次月经(LMP)后第7周结束时临床确认怀孕的女性中,数值染色体异常的估计比例为4.7%。如果足月时(活产和死产合并)数值染色体异常的频率为0.53%,那么这一频率要求第7周后发生的自然流产中有51.9%应是染色体异常的。自然流产调查的细胞遗传学数据显示发生率较低,为39.7%。然而,这个数字可能被低估了,因为在许多缺乏胚胎组织因而未进行核型分析的早期流产中,染色体异常几乎肯定被过度代表了。根据精子核型数据以及三体病因中母源和父源错误的相对频率信息,估算了减数分裂错误导致的受孕时数值染色体异常的频率。这提供了一个最低估计值,为20%。

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