Prenatal Ultrasound Suspicion of Cystic Fibrosis in a Multiethnic Population: Is Extensive
Africa
CFTR
Cystic Fibrosis (CF)
echogenic bowel
mutation
non-Caucasian
non-visualization of fetal gallbladder (NVFGB)
prenatal
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
29 04 2021
29 04 2021
Historique:
received:
04
03
2021
revised:
27
04
2021
accepted:
28
04
2021
entrez:
5
5
2021
pubmed:
6
5
2021
medline:
24
8
2021
Statut:
epublish
Résumé
In families without a Cystic Fibrosis (CF) history, fetal ultrasound bowel abnormalities can unexpectedly reveal the disease. Isolated or in association, the signs can be fetal bowel hyperechogenicity, intestinal loop dilatation and non-visualization of fetal gallbladder. In these cases, search for CF transmembrane conductance regulator (
Identifiants
pubmed: 33946859
pii: genes12050670
doi: 10.3390/genes12050670
pmc: PMC8145404
pii:
doi:
Substances chimiques
CFTR protein, human
0
Cystic Fibrosis Transmembrane Conductance Regulator
126880-72-6
Types de publication
Evaluation Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
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