Prenatal Lethal Diagnosis of 8p23.1 Duplication Syndrome Associated with Omphalocele and Encephalocele

Despite increased prenatal and postnatal use of array comparative genomic hybridization (aCGH), isolated 8p23.1 duplication remains rare and has been associated with a widely variable phenotype. Here, we report an isolated 8p23.1 duplication in a fetus with an omphalocele and encephalocele that were...

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Detalles Bibliográficos
Autores principales: Hicks, Melissa A., Ebrahim, Salah, Gonik, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985500/
https://www.ncbi.nlm.nih.gov/pubmed/36879850
http://dx.doi.org/10.1155/2023/5958223

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985500/
https://www.ncbi.nlm.nih.gov/pubmed/36879850
http://dx.doi.org/10.1155/2023/5958223

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