Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature

BACKGROUND: Trisomy of the short arm of chromosome 17 is a rare genomic disorder. The clinical features of complete trisomy 17p syndrome have been described. Most cases of this syndrome have been found in infants and children, but only a few cases were found by ultrasound in the prenatal period. MET...

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Detalles Bibliográficos
Autores principales: Li, Linlin, Zhang, Xinyue, Shi, Qingyang, Li, Leilei, Jiang, Yuting, Liu, Ruizhi, Zhang, Hongguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7843288/
https://www.ncbi.nlm.nih.gov/pubmed/32951212
http://dx.doi.org/10.1002/jcla.23582

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7843288/
https://www.ncbi.nlm.nih.gov/pubmed/32951212
http://dx.doi.org/10.1002/jcla.23582

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