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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,...

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Publicat a:Autops Case Rep
Autors principals: Costa, Andressa Dias, Schultz, Regina, Rosemberg, Sérgio
Format: Artigo
Idioma:Inglês
Publicat: São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2013
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6673682/
https://ncbi.nlm.nih.gov/pubmed/31528602
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4322/acr.2013.012
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