Fisher R A, Sheppard D M, Lawler S D
Br Med J (Clin Res Ed). 1982 Apr 24;284(6324):1218-20. doi: 10.1136/bmj.284.6324.1218.
In a case of complete hydatidiform mole with fetus the genetic origins were defined by the use of chromosomal polymorphisms. The fetus had a normal 46,XY karyotype with evidence of the presence of both maternal and paternal chromosomes. The mole was 46,XX and of androgenetic origin. There was no evidence of a maternal contribution, and duplication of paternal chromosomes was shown. In such atypical molar pregnancies examining genetic polymorphisms yields much more information than do sex chromosome studies and karyotyping, particularly in confirming the diagnosis and defining the origin and aetiology of the condition.
在一例伴有胎儿的完全性葡萄胎病例中,通过使用染色体多态性确定了其遗传起源。胎儿具有正常的46,XY核型,有证据表明存在母源和父源染色体。葡萄胎为46,XX,起源于雄核发育。没有母源贡献的证据,且显示有父源染色体的重复。在这种非典型的葡萄胎妊娠中,检查遗传多态性比性染色体研究和核型分析能提供更多信息,特别是在确诊以及确定病情的起源和病因方面。