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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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 |