Literature DB >> 33144663

Whole exome sequencing of fetal structural anomalies detected by ultrasonography.

Hiromi Aoi1,2, Takeshi Mizuguchi1, Toshifumi Suzuki2,3, Shintaro Makino2, Yuka Yamamoto2, Jun Takeda2, Yojiro Maruyama2, Rie Seyama1,2, Shiori Takeuchi2, Yuri Uchiyama1,4, Yoshiteru Azuma1, Kohei Hamanaka1, Atsushi Fujita1, Eriko Koshimizu1, Satoko Miyatake1,5, Satomi Mitsuhashi1, Atsushi Takata1, Noriko Miyake1, Satoru Takeda2, Atsuo Itakura2, Naomichi Matsumoto6.   

Abstract

The objective of this study was to evaluate the efficacy of whole exome sequencing (WES) for the genetic diagnosis of cases presenting with fetal structural anomalies detected by ultrasonography. WES was performed on 19 cases with prenatal structural anomalies. Genomic DNA was extracted from umbilical cords or umbilical blood obtained shortly after birth. WES data were analyzed on prenatal phenotypes alone, and the data were re-analyzed after information regarding the postnatal phenotype was obtained. Based solely on the fetal phenotype, pathogenic, or likely pathogenic, single nucleotide variants were identified in 5 of 19 (26.3%) cases. Moreover, we detected trisomy 21 in two cases by WES-based copy number variation analysis. The overall diagnostic rate was 36.8% (7/19). They were all compatible with respective fetal structural anomalies. By referring to postnatal phenotype information, another candidate variant was identified by a postnatal clinical feature that was not detected in prenatal screening. As detailed phenotyping is desirable for better diagnostic rates in WES analysis, we should be aware that fetal phenotype is a useful, but sometimes limited source of information for comprehensive genetic analysis. It is important to amass more data of genotype-phenotype correlations, especially to appropriately assess the validity of WES in prenatal settings.

Year:  2020        PMID: 33144663     DOI: 10.1038/s10038-020-00869-8

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  2 in total

1.  Morphological and ultrasonographic study of fetuses with cervical hygroma. A cases series.

Authors:  Octavian Munteanu; Monica Mihaela Cîrstoiu; Florin Mihail Filipoiu; Roxana Elena BohîlŢea; Ioan Alexandru Bulescu; Costin Berceanu
Journal:  Rom J Morphol Embryol       Date:  2016       Impact factor: 1.033

2.  Novel HSPG2 mutations causing Schwartz‑Jampel syndrome type 1 in a Chinese family: A case report.

Authors:  Wenjin Yan; Jin Dai; Dongquan Shi; Xingquan Xu; Xiao Han; Zhihong Xu; Dongyang Chen; Huajiang Teng; Qing Jiang
Journal:  Mol Med Rep       Date:  2018-06-06       Impact factor: 2.952

  2 in total
  6 in total

1.  Long-term course of early onset developmental and epileptic encephalopathy associated with 2q24.3 microduplication.

Authors:  Takuya Masuda; Hitoshi Osaka; Naomi Tsuchida; Satoko Miyatake; Kou Nishimura; Toshiki Takenouchi; Takao Takahashi; Naomichi Matsumoto; Takanori Yamagata
Journal:  Epilepsy Behav Rep       Date:  2022-04-25

2.  Intellectual disability and microcephaly associated with a novel CHAMP1 mutation.

Authors:  Yuta Asakura; Hitoshi Osaka; Hiromi Aoi; Takeshi Mizuguchi; Naomichi Matsumoto; Takanori Yamagata
Journal:  Hum Genome Var       Date:  2021-08-17

Review 3.  Prenatal Exome Sequencing: Background, Current Practice and Future Perspectives-A Systematic Review.

Authors:  Daniele Guadagnolo; Gioia Mastromoro; Francesca Di Palma; Antonio Pizzuti; Enrica Marchionni
Journal:  Diagnostics (Basel)       Date:  2021-02-02

4.  Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta-analysis.

Authors:  Rhiannon Mellis; Kathryn Oprych; Elizabeth Scotchman; Melissa Hill; Lyn S Chitty
Journal:  Prenat Diagn       Date:  2022-05-07       Impact factor: 3.242

Review 5.  Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges-Systematic Review of the Literature and Meta-Analysis.

Authors:  Gioia Mastromoro; Daniele Guadagnolo; Nader Khaleghi Hashemian; Enrica Marchionni; Alice Traversa; Antonio Pizzuti
Journal:  Diagnostics (Basel)       Date:  2022-02-23

6.  Clinical course of epilepsy and white matter abnormality linked to a novel DYRK1A variant.

Authors:  Tetsuya Okazaki; Hiroyuki Yamada; Kaori Matsuura; Noriko Kasagi; Noriko Miyake; Naomichi Matsumoto; Kaori Adachi; Eiji Nanba; Yoshihiro Maegaki
Journal:  Hum Genome Var       Date:  2021-07-12
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.