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Prenatal genetic diagnosis: fetal therapy as a possible solution to a positive test

BACKGROUND: Fetal abnormalities cause 20% of perinatal deaths. Advances in prenatal genetic and other types of screening offer great opportunities for identifying high risk pregnancies. METHODS: Through a literature search, here we summarise what are the prenatal diagnostic technique that are being...

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Autores principales: Kiani, Aysha Karim, Paolacci, Stefano, Scanzano, Pietro, Michelini, Sandro, Capodicasa, Natale, D’Agruma, Leonardo, Notarangelo, Angelantonio, Tonini, Gerolamo, Piccinelli, Daniela, Farshid, Kalantary Rad, Petralia, Paolo, Fulcheri, Ezio, Buffelli, Francesca, Chiurazzi, Pietro, Terranova, Corrado, Plotti, Francesco, Angioli, Roberto, Castori, Marco, Pös, Ondrej, Szemes, Tomas, Bertelli, Matteo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8023142/
https://www.ncbi.nlm.nih.gov/pubmed/33170180
http://dx.doi.org/10.23750/abm.v91i13-S.10534
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author Kiani, Aysha Karim
Paolacci, Stefano
Scanzano, Pietro
Michelini, Sandro
Capodicasa, Natale
D’Agruma, Leonardo
Notarangelo, Angelantonio
Tonini, Gerolamo
Piccinelli, Daniela
Farshid, Kalantary Rad
Petralia, Paolo
Fulcheri, Ezio
Buffelli, Francesca
Chiurazzi, Pietro
Terranova, Corrado
Plotti, Francesco
Angioli, Roberto
Castori, Marco
Pös, Ondrej
Szemes, Tomas
Bertelli, Matteo
author_facet Kiani, Aysha Karim
Paolacci, Stefano
Scanzano, Pietro
Michelini, Sandro
Capodicasa, Natale
D’Agruma, Leonardo
Notarangelo, Angelantonio
Tonini, Gerolamo
Piccinelli, Daniela
Farshid, Kalantary Rad
Petralia, Paolo
Fulcheri, Ezio
Buffelli, Francesca
Chiurazzi, Pietro
Terranova, Corrado
Plotti, Francesco
Angioli, Roberto
Castori, Marco
Pös, Ondrej
Szemes, Tomas
Bertelli, Matteo
author_sort Kiani, Aysha Karim
collection PubMed
description BACKGROUND: Fetal abnormalities cause 20% of perinatal deaths. Advances in prenatal genetic and other types of screening offer great opportunities for identifying high risk pregnancies. METHODS: Through a literature search, here we summarise what are the prenatal diagnostic technique that are being used and how those techniques may allow for prenatal interventions. RESULTS: Next generation sequencing and non-invasive prenatal testing are fundamental for clinical diagnostics because of their sensitivity and accuracy in identifying point mutations, aneuploidies, and microdeletions, respectively. Timely identification of genetic disorders and other fetal abnormalities enables early intervention, such as in-utero gene therapy, fetal drug therapy and prenatal surgery. CONCLUSION: Prenatal intervention is mainly focused on conditions that may cause death or lifelong disabilities, like spina bifida, congenital diaphragm hernia and sacrococcygeal teratoma; and may be an alternative therapeutic option to termination of pregnancy. However, it is not yet widely available, due to lack of specialized centers. (www.actabiomedica.it)
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spelling pubmed-80231422021-04-07 Prenatal genetic diagnosis: fetal therapy as a possible solution to a positive test Kiani, Aysha Karim Paolacci, Stefano Scanzano, Pietro Michelini, Sandro Capodicasa, Natale D’Agruma, Leonardo Notarangelo, Angelantonio Tonini, Gerolamo Piccinelli, Daniela Farshid, Kalantary Rad Petralia, Paolo Fulcheri, Ezio Buffelli, Francesca Chiurazzi, Pietro Terranova, Corrado Plotti, Francesco Angioli, Roberto Castori, Marco Pös, Ondrej Szemes, Tomas Bertelli, Matteo Acta Biomed Original Article BACKGROUND: Fetal abnormalities cause 20% of perinatal deaths. Advances in prenatal genetic and other types of screening offer great opportunities for identifying high risk pregnancies. METHODS: Through a literature search, here we summarise what are the prenatal diagnostic technique that are being used and how those techniques may allow for prenatal interventions. RESULTS: Next generation sequencing and non-invasive prenatal testing are fundamental for clinical diagnostics because of their sensitivity and accuracy in identifying point mutations, aneuploidies, and microdeletions, respectively. Timely identification of genetic disorders and other fetal abnormalities enables early intervention, such as in-utero gene therapy, fetal drug therapy and prenatal surgery. CONCLUSION: Prenatal intervention is mainly focused on conditions that may cause death or lifelong disabilities, like spina bifida, congenital diaphragm hernia and sacrococcygeal teratoma; and may be an alternative therapeutic option to termination of pregnancy. However, it is not yet widely available, due to lack of specialized centers. (www.actabiomedica.it) Mattioli 1885 2020 2020-11-09 /pmc/articles/PMC8023142/ /pubmed/33170180 http://dx.doi.org/10.23750/abm.v91i13-S.10534 Text en Copyright: © 2020 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Original Article
Kiani, Aysha Karim
Paolacci, Stefano
Scanzano, Pietro
Michelini, Sandro
Capodicasa, Natale
D’Agruma, Leonardo
Notarangelo, Angelantonio
Tonini, Gerolamo
Piccinelli, Daniela
Farshid, Kalantary Rad
Petralia, Paolo
Fulcheri, Ezio
Buffelli, Francesca
Chiurazzi, Pietro
Terranova, Corrado
Plotti, Francesco
Angioli, Roberto
Castori, Marco
Pös, Ondrej
Szemes, Tomas
Bertelli, Matteo
Prenatal genetic diagnosis: fetal therapy as a possible solution to a positive test
title Prenatal genetic diagnosis: fetal therapy as a possible solution to a positive test
title_full Prenatal genetic diagnosis: fetal therapy as a possible solution to a positive test
title_fullStr Prenatal genetic diagnosis: fetal therapy as a possible solution to a positive test
title_full_unstemmed Prenatal genetic diagnosis: fetal therapy as a possible solution to a positive test
title_short Prenatal genetic diagnosis: fetal therapy as a possible solution to a positive test
title_sort prenatal genetic diagnosis: fetal therapy as a possible solution to a positive test
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8023142/
https://www.ncbi.nlm.nih.gov/pubmed/33170180
http://dx.doi.org/10.23750/abm.v91i13-S.10534
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