Prenatal diagnosis of syndromic alobar holoprosencephaly associated with digynic triploidy fetus

Holoprosencephaly (HPE) is a dramatic human brain malformation sequence with an extreme variable phenotypic spectrum and genetic heterogeneity, variable degree of severity and unknown etiology, in many cases. HPE is classified into syndromic, chromosomal, and non-syndromic, non-chromosomal. The most...

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Detalles Bibliográficos
Autores principales: Albu, Cristina-Crenguţa, Albu, Dinu-Florin, Pătraşcu, Anca, Albu, Ştefan Dimitrie, Efrem, Ion Cristian, Gogănău, Alexandru Marian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343603/
https://www.ncbi.nlm.nih.gov/pubmed/34171079
http://dx.doi.org/10.47162/RJME.61.4.32

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343603/
https://www.ncbi.nlm.nih.gov/pubmed/34171079
http://dx.doi.org/10.47162/RJME.61.4.32

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