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史密斯-勒米-奥皮茨综合征携带者频率及宫内死亡率估计

Smith-Lemli-Opitz syndrome carrier frequency and estimates of in utero mortality rates.

作者信息

Lazarin Gabriel A, Haque Imran S, Evans Eric A, Goldberg James D

机构信息

Counsyl, South San Francisco, CA, USA.

出版信息

Prenat Diagn. 2017 Apr;37(4):350-355. doi: 10.1002/pd.5018. Epub 2017 Mar 9.

Abstract

OBJECTIVE

To tabulate individual allele frequencies and total carrier frequency for Smith-Lemli-Opitz syndrome (SLOS) and compare expected versus observed birth incidences.

METHODS

A total of 262 399 individuals with no known indication or increased probability of SLOS carrier status, primarily US based, were screened for SLOS mutations as part of an expanded carrier screening panel. Results were retrospectively analyzed to estimate carrier frequencies in multiple ethnic groups. SLOS birth incidences obtained from existing literature were then compared with these data to estimate the effect of SLOS on fetal survival.

RESULTS

Smith-Lemli-Opitz syndrome carrier frequency is highest in Ashkenazi Jews (1 in 43) and Northern Europeans (1 in 54). Comparing predicted birth incidence with that observed in published literature suggests that approximately 42% to 88% of affected conceptuses experience prenatal demise.

CONCLUSION

Smith-Lemli-Opitz syndrome is relatively frequent in certain populations and, because of its impact on prenatal and postnatal morbidity and mortality, merits consideration for routine screening. © 2017 The Authors. Prenatal Diagnosis published by John Wiley & Sons, Ltd.

摘要

目的

列出史密斯-勒米-奥皮茨综合征(SLOS)的个体等位基因频率和总携带者频率,并比较预期与观察到的出生发病率。

方法

作为扩大携带者筛查 panel 的一部分,对总共262399名无已知 SLOS 携带者状态指征或患病概率增加的个体进行了 SLOS 突变筛查,这些个体主要来自美国。对结果进行回顾性分析,以估计多个种族群体中的携带者频率。然后将从现有文献中获得的 SLOS 出生发病率与这些数据进行比较,以估计 SLOS 对胎儿存活的影响。

结果

史密斯-勒米-奥皮茨综合征携带者频率在阿什肯纳兹犹太人中最高(43人中有1人),在北欧人中其次(54人中有1人)。将预测的出生发病率与已发表文献中观察到的发病率进行比较表明,约42%至88%的受影响胎儿会在产前死亡。

结论

史密斯-勒米-奥皮茨综合征在某些人群中相对常见,并且由于其对产前和产后发病率及死亡率的影响,值得考虑进行常规筛查。© 2017作者。《产前诊断》由约翰·威利父子有限公司出版。

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