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False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY

Introduction  Pentasomy 49,XXXXY is a sex chromosome anomaly difficult to be diagnosed prenatally. We describe a patient of pentasomy 49,XXXXY with false low-risk results using a noninvasive prenatal screening (NIPS). A 30-year-old G1P0 woman presented at 33 (6/7) weeks, secondary to sonographic fet...

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Autores principales: Putra, Manesha, Hicks, Melissa A., Abramowicz, Jacques S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical Publishers 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775094/
https://www.ncbi.nlm.nih.gov/pubmed/29362687
http://dx.doi.org/10.1055/s-0037-1621722
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author Putra, Manesha
Hicks, Melissa A.
Abramowicz, Jacques S.
author_facet Putra, Manesha
Hicks, Melissa A.
Abramowicz, Jacques S.
author_sort Putra, Manesha
collection PubMed
description Introduction  Pentasomy 49,XXXXY is a sex chromosome anomaly difficult to be diagnosed prenatally. We describe a patient of pentasomy 49,XXXXY with false low-risk results using a noninvasive prenatal screening (NIPS). A 30-year-old G1P0 woman presented at 33 (6/7) weeks, secondary to sonographic fetal anomalies. She had low-risk NIPS at 13 (6/7) weeks. Anatomy survey showed bilateral clubfeet, clinodactyly of the left fifth digit, micropenis, and echogenic bowel. Cytogenetics analysis revealed pentasomy 49,XXXXY syndrome. We report third-trimester sonographic features of a fetus with pentasomy 49,XXXXY and the importance of thorough pre- and posttest counseling for NIPS.
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spelling pubmed-57750942018-01-23 False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY Putra, Manesha Hicks, Melissa A. Abramowicz, Jacques S. AJP Rep Introduction  Pentasomy 49,XXXXY is a sex chromosome anomaly difficult to be diagnosed prenatally. We describe a patient of pentasomy 49,XXXXY with false low-risk results using a noninvasive prenatal screening (NIPS). A 30-year-old G1P0 woman presented at 33 (6/7) weeks, secondary to sonographic fetal anomalies. She had low-risk NIPS at 13 (6/7) weeks. Anatomy survey showed bilateral clubfeet, clinodactyly of the left fifth digit, micropenis, and echogenic bowel. Cytogenetics analysis revealed pentasomy 49,XXXXY syndrome. We report third-trimester sonographic features of a fetus with pentasomy 49,XXXXY and the importance of thorough pre- and posttest counseling for NIPS. Thieme Medical Publishers 2018-01 2018-01-19 /pmc/articles/PMC5775094/ /pubmed/29362687 http://dx.doi.org/10.1055/s-0037-1621722 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Putra, Manesha
Hicks, Melissa A.
Abramowicz, Jacques S.
False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY
title False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY
title_full False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY
title_fullStr False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY
title_full_unstemmed False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY
title_short False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY
title_sort false low-risk single nucleotide polymorphism–based noninvasive prenatal screening in pentasomy 49,xxxxy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775094/
https://www.ncbi.nlm.nih.gov/pubmed/29362687
http://dx.doi.org/10.1055/s-0037-1621722
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