High rate of twins among offspring of mothers with the Järvi-Hakola-Nasu disease and with comments on disorders associated with twinning.

H P Hakola, A W Eriksson
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引用次数: 0

Abstract

Finnish mothers with Jrvi-Hakola-Nasu disease, progressive dementia with lipomembranous polycystic osteodysplasia (McKusick 221770) have a high rate of twin maternities, 128.2/1000. The exact 99% confidence intervals are 28.7-322.2/1000, thus above the average twinning rate in Finland, i.e. 15/1000. This eightfold increase in twinning may be an indication of a disturbed cortico-hypothalmic-hypophyseal axis or an other premorbid hormonal imbalance. It is concluded that even if dizygotic twinning is as a rule an event in itself, not only iatrogenic factors, as ovulation inducers, etc., but also some genetic disorders may be associated with twinning. More studies are needed to elucidate the incidence of twinning in families with these disorders.

患有Järvi-Hakola-Nasu疾病的母亲的后代双胞胎率高,并对与双胞胎有关的疾病发表评论。
患有Jrvi-Hakola-Nasu病、进行性痴呆伴脂膜性多囊性骨质增生(McKusick 221770)的芬兰母亲的双胞胎发生率很高,为128.2/1000。确切的99%置信区间为28.7-322.2/1000,因此高于芬兰的平均孪生率,即15/1000。这八倍的双胞胎增加可能是皮质-下丘脑-垂体轴紊乱或其他病前激素失衡的迹象。综上所述,即使异卵双胞胎本身是一个规律事件,但除了医源性因素,如促排卵剂等,一些遗传疾病也可能与双胞胎有关。需要更多的研究来阐明双胞胎在这些疾病家庭中的发生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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