1.
Clin Case Rep
; 9(12): e05163, 2021 Dec.
Artículo
en Inglés
| MEDLINE
| ID: mdl-34987809
RESUMEN
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 congenital anomalies including diprosopus and discusses the implications of prenatal diagnosis.