Proposal for Practical Approach in Prenatal Diagnosis of Beckwith–Wiedemann Syndrome and Review of the Literature

Background: Beckwith–Wiedemann syndrome (BWS) is a phenotypically and genetically heterogeneous disorder associated with epigenetic/genetic aberrations on chromosome 11p15.4p15.5. There is no consensus criterion for prenatal diagnosis of BWS. Methods: Three BWS patients with their clinical histories...

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Detalles Bibliográficos
Autores principales: Ma, Gwo-Chin, Chen, Tze-Ho, Wu, Wan-Ju, Lee, Dong-Jay, Lin, Wen-Hsiang, Chen, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315620/
https://www.ncbi.nlm.nih.gov/pubmed/35885613
http://dx.doi.org/10.3390/diagnostics12071709

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315620/
https://www.ncbi.nlm.nih.gov/pubmed/35885613
http://dx.doi.org/10.3390/diagnostics12071709

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