[EUROCAT研究中选定的产前畸形数据]苏黎世州1988 - 1997年的结果]。

S Achermann, M C Addor, A Schinzel
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引用次数: 0

摘要

在EUROCAT研究的背景下,从苏黎世州(1988-1997)收集了选定的先天性畸形和染色体畸变的数据。结果发现,严重和早期畸形,如无脑和前脑畸形,以产前检出为主;对于唇腭裂和脑脊膜膨出,情况并非如此,至少在孤立的(非综合征)畸形方面是如此。然而,如果这些缺陷与染色体畸变同时发生,这种情况被登记的可能性更高。同样的原因,由于超声异常和宫内发育迟缓,13和18三体比21三体更容易在产前被发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Data on selected prenatal malformations in the EUROCAT study. Results of Zurich Canton from 1988 to 1997].

In the context of the EUROCAT study, data on selected congenital malformations and chromosome aberrations were collected from the Canton of Zurich (1988-1997). It was found that the major proportion of severe and early malformations, such as anencephalus and holoprosencephaly, were detected prenatally; for oral clefts and meningomyeloceles this was not the case, at any rate in regard to isolated (non-syndromic) malformations. However, if these defects occur in combination with a chromosome aberration, the likelihood of such a case being registered is higher. For the same reason, i.e. due to abnormal ultrasound findings and intrauterine growth retardation, trisomies 13 and 18 were more often detected prenatally than trisomy 21.

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