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Genetics in prenatal diagnosis

The options for prenatal genetic testing have evolved rapidly in the past decade, and advances in sequencing technology now allow genetic diagnoses to be made down to the single-base-pair level, even before the birth of the child. This offers women the opportunity to obtain information regarding the...

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Autores principales: Lim, Karen Mei Xian, Mahyuddin, Aniza Puteri, Gosavi, Arundhati Tushar, Choolani, Mahesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979796/
https://www.ncbi.nlm.nih.gov/pubmed/36722514
http://dx.doi.org/10.4103/singaporemedj.SMJ-2021-433
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author Lim, Karen Mei Xian
Mahyuddin, Aniza Puteri
Gosavi, Arundhati Tushar
Choolani, Mahesh
author_facet Lim, Karen Mei Xian
Mahyuddin, Aniza Puteri
Gosavi, Arundhati Tushar
Choolani, Mahesh
author_sort Lim, Karen Mei Xian
collection PubMed
description The options for prenatal genetic testing have evolved rapidly in the past decade, and advances in sequencing technology now allow genetic diagnoses to be made down to the single-base-pair level, even before the birth of the child. This offers women the opportunity to obtain information regarding the foetus, thereby empowering them to make informed decisions about their pregnancy. As genetic testing becomes increasingly available to women, clinician knowledge and awareness of the options available to women is of great importance. Additionally, comprehensive pretest and posttest genetic counselling about the advantages, pitfalls and limitations of genetic testing should be provided to all women. This review article aims to cover the range of genetic tests currently available in prenatal screening and diagnosis, their current applications and limitations in clinical practice as well as what the future holds for prenatal genetics.
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spelling pubmed-99797962023-03-03 Genetics in prenatal diagnosis Lim, Karen Mei Xian Mahyuddin, Aniza Puteri Gosavi, Arundhati Tushar Choolani, Mahesh Singapore Med J Review Article The options for prenatal genetic testing have evolved rapidly in the past decade, and advances in sequencing technology now allow genetic diagnoses to be made down to the single-base-pair level, even before the birth of the child. This offers women the opportunity to obtain information regarding the foetus, thereby empowering them to make informed decisions about their pregnancy. As genetic testing becomes increasingly available to women, clinician knowledge and awareness of the options available to women is of great importance. Additionally, comprehensive pretest and posttest genetic counselling about the advantages, pitfalls and limitations of genetic testing should be provided to all women. This review article aims to cover the range of genetic tests currently available in prenatal screening and diagnosis, their current applications and limitations in clinical practice as well as what the future holds for prenatal genetics. Wolters Kluwer - Medknow 2023-01-19 /pmc/articles/PMC9979796/ /pubmed/36722514 http://dx.doi.org/10.4103/singaporemedj.SMJ-2021-433 Text en Copyright: © 2023 Singapore Medical Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Lim, Karen Mei Xian
Mahyuddin, Aniza Puteri
Gosavi, Arundhati Tushar
Choolani, Mahesh
Genetics in prenatal diagnosis
title Genetics in prenatal diagnosis
title_full Genetics in prenatal diagnosis
title_fullStr Genetics in prenatal diagnosis
title_full_unstemmed Genetics in prenatal diagnosis
title_short Genetics in prenatal diagnosis
title_sort genetics in prenatal diagnosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979796/
https://www.ncbi.nlm.nih.gov/pubmed/36722514
http://dx.doi.org/10.4103/singaporemedj.SMJ-2021-433
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