Suppr超能文献

如何处理孕期雌三醇水平偏低:单中心经验

How to Manage Low Estriol Levels in Pregnancies, One Center Experience.

作者信息

Yilmaz Gulec Elif, Gezdirici Alper, Ayaz Akif, Ozturk Fatma Nihal, Polat Ibrahim

机构信息

Istanbul Medeniyet University Medical School, Department of Medical Genetics, Istanbul, Turkey.

University of Health Sciences Turkey, Basaksehir Cam and Sakura City Hospital, Clinic of Medical Genetics, Istanbul, Turkey.

出版信息

Medeni Med J. 2022 Mar 18;37(1):62-70. doi: 10.4274/MMJ.galenos.2022.22747.

Abstract

OBJECTIVE

Low estriol (uE3) levels in the second-trimester screening for Down syndrome may be the result of fetal demise, congenital abnormalities, or some genetic hormonal disorders of the fetus. Although X-linked ichthyosis, a microdeletion syndrome with mild ichthyosis, which causes steroid sulfatase (STS) deficiency, is the most common genetic cause, second-trimester screening tests calculate the risk for a less common and severe disorder known as the Smith Lemli Opitz syndrome (SLOS). We aimed to investigate the outcomes of pregnancies with low uE3 levels in Down syndrome screening and emphasize the high prevalence of STS deficiency instead of SLOS in such cases.

METHODS

Fifteen pregnancies with very low uE3 levels and high risk for trisomy and/or SLOS in screening tests were evaluated and tested for STS deficiency and SLOS.

RESULTS

Seven of the pregnancies had STS microdeletion syndrome, while additional two cases were supposed to have STS gene mutation according to family and/or postnatal history. Although one fetal death was recorded, no chromosomal abnormality, SLOS, or congenital malformation was recorded in our series.

CONCLUSIONS

SLOS is a very severe and rare syndrome. The risk estimation for SLOS in screening tests causes stress for pregnant women and healthcare givers. We recommend the addition of risk estimation for STS deficiency when a low uE3 level is detected in the screening test.

摘要

目的

在孕中期唐氏综合征筛查中,雌三醇(uE3)水平低可能是胎儿死亡、先天性异常或胎儿某些遗传性激素紊乱的结果。虽然X连锁鱼鳞病是一种伴有轻度鱼鳞病的微缺失综合征,可导致类固醇硫酸酯酶(STS)缺乏,是最常见的遗传原因,但孕中期筛查测试计算的是一种较罕见且严重的疾病——史密斯-勒米-奥皮茨综合征(SLOS)的风险。我们旨在调查唐氏综合征筛查中uE3水平低的妊娠结局,并强调在此类情况下STS缺乏的高患病率而非SLOS。

方法

对15例筛查试验中uE3水平极低且三体和/或SLOS风险高的妊娠进行评估,并检测STS缺乏和SLOS。

结果

7例妊娠患有STS微缺失综合征,另外2例根据家族和/或产后病史推测有STS基因突变。虽然记录了1例胎儿死亡,但我们的系列中未记录到染色体异常、SLOS或先天性畸形。

结论

SLOS是一种非常严重且罕见的综合征。筛查试验中对SLOS的风险评估给孕妇和医护人员带来压力。我们建议在筛查试验中检测到uE3水平低时增加对STS缺乏的风险评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4450/8939441/c670cf144170/medj-37-62-g1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验