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由于三体拯救导致的 21 号单亲二体病例中,胎儿核型分析与母体外周血游离胎儿 DNA 测序无创产前检测结果不一致。

Discordant results between fetal karyotyping and non-invasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic rescue.

机构信息

Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou, Guangdong, China.

出版信息

Prenat Diagn. 2013 Jun;33(6):598-601. doi: 10.1002/pd.4069. Epub 2013 Mar 27.

Abstract

Uniparental disomy (UPD) is an uncommon chromosome condition, but UPD involving chromosome 21 is rarely reported. We reported here a case who had first trimester screening test for Down syndrome, chorionic villus sampling for fetal karyotyping, quantitative fluorescence polymerase chain reaction (QF-PCR), as well as non-invasive prenatal testing (NIPT) by maternal plasma sequencing. There were discordant results between fetal karyotyping and NIPT due to UPD 21combined with confined placental mosaicism of trisomy 21. This demonstrated that it is possible to detect placental mosaicism by NIPT, but further studies are required to confirm its sensitivity. Therefore, all positive NIPT results must be confirmed by conventional invasive test and karyotyping. QF-PCR has the additional benefit in diagnosing UPD.

摘要

单亲二体(UPD)是一种罕见的染色体疾病,但涉及 21 号染色体的 UPD 则很少报道。我们在此报告一例患者,该患者曾行唐氏综合征早孕期筛查、绒毛活检行胎儿染色体核型分析、荧光定量聚合酶链反应(QF-PCR)以及母体外周血游离胎儿 DNA 测序的无创产前检测(NIPT)。由于 21 号染色体 UPD 合并局限性胎盘嵌合三体 21,胎儿染色体核型分析与 NIPT 的结果不一致。这表明 NIPT 有可能检测到胎盘嵌合体,但需要进一步的研究来确认其敏感性。因此,所有阳性的 NIPT 结果必须通过常规的有创性检测和核型分析来证实。QF-PCR 在诊断 UPD 方面具有额外的优势。

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