Genetic Background of Fetal Growth Restriction.
chromosomal microarray
fetal growth restriction
genetics
single nucleotide polymorphism
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
21 Dec 2021
21 Dec 2021
Historique:
received:
18
10
2021
revised:
17
12
2021
accepted:
19
12
2021
entrez:
11
1
2022
pubmed:
12
1
2022
medline:
29
1
2022
Statut:
epublish
Résumé
Fetal growth restriction (FGR) is one of the most formidable challenges in present-day antenatal care. Pathological fetal growth is a well-known factor of not only in utero demise in the third trimester, but also postnatal morbidity and unfavorable developmental outcomes, including long-term sequalae such as metabolic diseases, diabetic mellitus or hypertension. In this review, the authors present the current state of knowledge about the genetic disturbances responsible for FGR diagnosis, divided into fetal, placental and maternal causes (including preeclampsia), as well as their impact on prenatal diagnostics, with particular attention on chromosomal microarray (CMA) and noninvasive prenatal testing technique (NIPT).
Identifiants
pubmed: 35008459
pii: ijms23010036
doi: 10.3390/ijms23010036
pmc: PMC8744929
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Ministry of Science and Higher Education
ID : OPK 510-18-83
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