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Preterm infant with diprosopus and holoprosencephaly

Diprosopus is an extremely rare congenital anomaly involving craniofacial duplication. The etiology and pathophysiology remain unknown, and no genetic mutations have been definitively associated with the condition. This case describes an infant born at 27‐weeks completed gestation with multiple cong...

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Detalles Bibliográficos
Autores principales: Nair, Nitya M., Swarr, Daniel T., Barnes‐Davis, Maria E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695654/
https://www.ncbi.nlm.nih.gov/pubmed/34987809
http://dx.doi.org/10.1002/ccr3.5163