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Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic Abnormalities

机译:超声检查未发现异常的情况下,马赛克18p四联体的产前诊断。

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摘要

Small supernumerary marker chromosomes (sSMC) are still a major problem in clinical cytogenetics as they cannot be identified or characterized unambiguously by conventional cytogenetics alone. On the other hand, and perhaps more importantly in prenatal settings, there is a challenging situation for counseling how to predict the risk for an abnormal phenotype, especially in cases with a de novo sSMC. Here we report on the prenatal diagnosis of a mosaic tetrasomy 18p due to presence of an sSMC in a fetus without abnormal sonographic signs. For a 26-year-old, gravida 2 (para 1) amniocentesis was done due to consanguineous marriage and concern for Down syndrome, based on borderline risk assessment. Parental karyotypes were normal, indicating a de novo chromosome aberration of the fetus. FISH analysis as well as molecular karyotyping identified the sSMC as an i(18)(pter->q10:q10->pter), compatible with tetrasomy for the mentioned region. Cordocentesis was done due to normal sonography and the results from amniocentesis were confirmed. The parents opted for pregnancy termination and post mortem examination now noted, low anterior hairline, large philtrum, low-set posteriorly rotated malformed ears with prominent antihelix, lower limbs joint contracture and digital anomalies, including long and narrow toes with clinodactyly of the 1st and 5th toes and postaxial polydactyly of one hand. De novo i(18p) can be considered as a special case in the sense that the major relevant phenotypes mentioned for it, i.e. feeding difficulties, abnormalities in muscle tone and developmental/mental retardation, cognitive and behavioral characteristics, recurrent otitis media and seizures, are mostly postnatal. This emphasizes the necessity to determine the nature of a de novo euchromatic marker chromosome, especially in cases with normal ultrasound result and the suitability of a cordocentesis in order to better predicting the pregnancy outcome and parental counseling.
机译:小数目标记染色体(sSMC)仍然是临床细胞遗传学中的主要问题,因为它们不能仅通过常规细胞遗传学来明确鉴定或表征。另一方面,也许更重要的是在产前环境中,如何建议如何预测异常表型的风险,尤其是在患有新生sSMC的情况下,存在着挑战性的局面。在这里,我们报告了由于在没有异常超声征象的胎儿中存在sSMC而导致的马赛克四体性18p的产前诊断。根据边界风险评估,由于近亲结婚和对唐氏综合症的关注,对一名26岁的孕妇进行了gravida 2(第1段)羊膜穿刺术。父母的核型是正常的,表明胎儿的从头染色体畸变。 FISH分析以及分子核型分析确定sSMC为i(18)(pter-> q10:q10-> pter),与上述区域的四体性相容。由于超声检查正常,进行了穿刺穿刺术,并确认了羊膜穿刺术的结果。父母现在选择终止妊娠并进行验尸检查,前发际线低,腓骨大,低位后旋转畸形耳朵,突出的抗螺旋结构,下肢关节挛缩和数字异常,包括长而窄的脚趾,倾斜度为1。一只脚的sup> st 和第5 脚趾和后轴多指。从头来说,De novo i(18p)被认为是特例,因为它涉及到主要的相关表型,即进食困难,肌张力和发育/智力发育异常,认知和行为特征,中耳炎反复发作和癫痫发作,多产后。这强调了确定从头正常染色体标记染色体的性质的必要性,特别是在超声检查结果正常且需要进行脐带穿刺术的情况下,以便更好地预测妊娠结果和父母咨询。

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