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
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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Auteurs

Nicoletta Villa (N)

UC Medical Genetics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.

Serena Redaelli (S)

School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

Stefania Farina (S)

UC Medical Genetics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.
School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

Elena Sala (E)

UC Medical Genetics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.

Francesca Crosti (F)

UC Medical Genetics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.

Sabrina Cozzolino (S)

Department of Obstetrics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.

Maria Verderio (M)

Department of Obstetrics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.

Leda Dalprà (L)

UC Medical Genetics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.
School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

Gaia Roversi (G)

UC Medical Genetics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.
School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

Angela Bentivegna (A)

School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

Giovanni Cazzaniga (G)

UC Medical Genetics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.
School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

Marialuisa Lavitrano (M)

School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

Donatella Conconi (D)

School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.

Classifications MeSH