Mitra Anjali, Dolitsky Shelley, Yadava Stacy, Ashkinadze Elena
Department of Obstetrics, Gynecology and Reproductive Sciences, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey.
AJP Rep. 2020 Jan;10(1):e118-e120. doi: 10.1055/s-0040-1705131. Epub 2020 Mar 31.
Based on the known carrier frequency of Smith-Lemli-Opitz's syndrome (SLOS), the prevalence of this disease should be significantly higher than what is observed in the population. This may be due to a higher rate of pregnancy loss in affected embryos. Here, we present the case of a couple who underwent expanded carrier screening (ECS) after experiencing three first trimester pregnancy losses. Both parents were found to be carriers of SLOS mutations, and DNA analysis of the fetal remains of the third loss revealed the aborted fetus had inherited both the maternal and paternal mutations. This suggests SLOS as a reason for this patient's recurrent pregnancy loss (RPL), and therefore, ECS should be considered as part of the RPL work-up.
基于已知的史密斯-利姆利-奥皮茨综合征(SLOS)携带者频率,该疾病的患病率应显著高于在人群中观察到的情况。这可能是由于受影响胚胎的妊娠丢失率较高。在此,我们介绍一对夫妇的病例,他们在经历了三次孕早期妊娠丢失后接受了扩展携带者筛查(ECS)。发现父母双方均为SLOS突变的携带者,对第三次妊娠丢失的胎儿遗体进行的DNA分析显示,流产胎儿继承了母系和父系的突变。这表明SLOS是该患者复发性妊娠丢失(RPL)的一个原因,因此,ECS应被视为RPL检查的一部分。