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小脑延髓池增大作为低风险亚洲人群染色体异常的一个指标。

Enlargement of cisterna magna as an indicator of chromosomal abnormalities in a low-risk Asian population.

作者信息

Ek S, Anadakumar C, Wong Y C, Chau T M, Gole L A, Malarvishy G

机构信息

Department of Obstetrics and Gynecology, National University of Singapore.

出版信息

J Perinat Med. 1998;26(4):325-7. doi: 10.1515/jpme.1998.26.4.325.

Abstract

AIMS

The aims of this study was to invent the prevalence of cisterna magna (CM) enlargement in a low-risk population and relate this to chromosomal abnormalities and initial delivery outcome.

STUDY DESIGN

11,145 patients having routine ultrasound scan at 21st week of pregnancy were screened for abnormalities. Cases with CM enlargement were traced and outcome retrieved either from case notes or from the patients.

RESULTS

In our low-risk population six fetuses were found to have CM enlargement. Only one had a chromosomal abnormality, 47XY + 18, and this fetus also presented with other malformations. Four were healthy at birth and one, also with other malformations, is showing signs of mental retardation. All cases were male.

CONCLUSION

Isolated CM enlargement does not seems to be an indicator for chromosomal abnormalities, especially if the fetus is a male. Still, it should alert the examiner of the possibility of other malformations, which may be of importance.

摘要

目的

本研究旨在确定低风险人群中枕大池(CM)扩大的患病率,并将其与染色体异常和初次分娩结局相关联。

研究设计

对11145例在妊娠21周时进行常规超声扫描的患者进行异常筛查。对枕大池扩大的病例进行追踪,并从病例记录或患者处获取结局。

结果

在我们的低风险人群中,发现6例胎儿存在枕大池扩大。仅1例有染色体异常,47XY + 18,且该胎儿还伴有其他畸形。4例出生时健康,1例也伴有其他畸形,现显示出智力发育迟缓的迹象。所有病例均为男性。

结论

孤立性枕大池扩大似乎不是染色体异常的指标,尤其是当胎儿为男性时。不过,它仍应提醒检查者注意其他畸形的可能性,这可能很重要。

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