Prenatal phenotype of Wolf–Hirschhorn syndrome: A case series and literature review

OBJECTIVE: Wolf–Hirschhorn syndrome (WHS) is a congenital malformation syndrome with poor prognosis. It is associated with a heterozygous deletion of chromosome 4p16.3. Adequate knowledge of prenatal phenotypes and proper prenatal counseling are essential for intrauterine diagnosis. METHOD: We retro...

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Detalles Bibliográficos
Autores principales: Tang, Feng, Zeng, Yang, Wang, Li, Yin, Daishu, Chen, Lin, Xie, Dan, Wang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265096/
https://www.ncbi.nlm.nih.gov/pubmed/36849216
http://dx.doi.org/10.1002/mgg3.2155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265096/
https://www.ncbi.nlm.nih.gov/pubmed/36849216
http://dx.doi.org/10.1002/mgg3.2155

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