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Alobar holoprosencephaly and Trisomy 13 (Patau syndrome)
Holoprosencephaly (HPE) is a congenital defect of the brain, median structures, and face resulting from an incomplete cleavage of the primitive brain during early embryogenesis. The authors report a case of trisomy 13 syndrome diagnosed at prenatal follow up. The preterm newborn lived only 5 hours,...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
São Paulo, SP: Universidade de São Paulo, Hospital Universitário
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6673682/ https://www.ncbi.nlm.nih.gov/pubmed/31528602 http://dx.doi.org/10.4322/acr.2013.012 |