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家族性葡萄胎的遗传异质性证据。

Evidence of a genetic heterogeneity of familial hydatidiform moles.

作者信息

Slim R, Fallahian M, Rivière J-B, Zali M R

机构信息

Department of Human Genetics, McGill University Health Center, Montreal, Canada H3G 1A4.

出版信息

Placenta. 2005 Jan;26(1):5-9. doi: 10.1016/j.placenta.2004.04.001.

Abstract

We previously mapped a maternal recessive locus responsible for familial hydatidiform moles (HMs) to 19q13.4. The candidate region has recently been narrowed down to 1.1 megabases. Here, we report the segregation of alleles at 18 genetic markers, including nine new ones, from the HMs candidate region in a recently reported consanguineous family. In this family, five affected women had a total of seven HMs, three miscarriages, and three normal children. Linkage and haplotype analyses exclude linkage to 19q13.4 and indicate the presence of a second recessive locus responsible for familial molar pregnancies. The heterogeneity in the phenotype of the conceptuses of patients with familial HMs is in agreement with previous observations and seems to be a common feature of this condition. This indicates that the homozygous genetic defects leading to hydatidiform moles can be modulated by other genetic or environmental factors. The identification of these factors may unravel natural ways to treat these forms of reproductive wastage and reverse the infertility of women with recurrent moles.

摘要

我们之前将一个导致家族性葡萄胎(HM)的母系隐性基因座定位到19q13.4。该候选区域最近已缩小至1.1兆碱基。在此,我们报告了一个最近报道的近亲家庭中18个遗传标记(包括9个新标记)的等位基因分离情况,这些标记来自HM候选区域。在这个家庭中,5名受影响的女性共有7次葡萄胎、3次流产和3个正常孩子。连锁和单倍型分析排除了与19q13.4的连锁关系,并表明存在第二个导致家族性葡萄胎妊娠的隐性基因座。家族性HM患者妊娠产物表型的异质性与之前的观察结果一致,似乎是这种疾病的一个共同特征。这表明导致葡萄胎的纯合基因缺陷可能受到其他遗传或环境因素的调节。识别这些因素可能会揭示治疗这些形式生殖浪费的自然方法,并逆转复发性葡萄胎女性的不孕状况。

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