Cytogenetically Balanced Reciprocal Translocation Could Hide Molecular Genomic Unbalances: Implications for Foetal Phenotype Correlation.
PEX3 gene
chromosomal translocation
cytogenetic analysis
genomic comparative hybridisation array
genomic deletion
prenatal diagnosis
Journal
Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402
Informations de publication
Date de publication:
09 Aug 2024
09 Aug 2024
Historique:
received:
10
07
2024
revised:
02
08
2024
accepted:
08
08
2024
medline:
31
8
2024
pubmed:
31
8
2024
entrez:
29
8
2024
Statut:
epublish
Résumé
When an increased nuchal translucency (>3.00 mm) is observed during the echographic examination of a foetus in the first trimester of pregnancy, an increased risk of chromosomopathy is considered, and the pregnant woman is offered the possibility of an invasive investigation. Here, we focused our attention on prenatal diagnosis issues in cases of foetuses with cytogenetically balanced reciprocal translocations. We report the finding of a cytogenetically balanced, de facto genomically unbalanced translocation that poses a challenge in a case of prenatal diagnosis, changing the risk of Down syndrome in a Zellweger syndromic spectrum risk (
Identifiants
pubmed: 39202220
pii: diagnostics14161732
doi: 10.3390/diagnostics14161732
pmc: PMC11353226
pii:
doi:
Types de publication
Journal Article
Langues
eng
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