Faber G, Witkowski R, Zieger U, Weber K, Wrassmann U
Zentralbl Gynakol. 1980;102(4):239-43.
Prenatal amniocentesis, chromosome analysis, as well as clinical and pathologicoanatomic approaches are some of the ways by which to diagnose triploidy. The methods are described against the background of triploidy (karyotype 69 XXX) in a bipara, 24 years of age. Prenatal examination of hydramnion, particularly in cases with concomitant gestosis, should include amnion cell culturing for early detection of triploidy. Postnatal diagnosis, in response to typical malformation of the foetus and placenta, is possible, provided that thought is given to that aspect.
产前羊膜穿刺术、染色体分析以及临床和病理解剖学方法是诊断三倍体的一些途径。这些方法是在一名24岁经产妇三倍体（核型69 XXX）的背景下进行描述的。产前检查羊水过多时，尤其是伴有妊娠中毒症的情况，应包括羊膜细胞培养以便早期发现三倍体。如果考虑到这方面，产后根据胎儿和胎盘的典型畸形进行诊断是可行的。
