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A omphalocele associated with multiple congenital anomalies is extremely rare congenital malformation.
We experienced a ruptured large omphalocele of short duration associated with multiple congenital anomalies such as patent omphalomesenteric duct, cleft palate and lip, postaxial polydactylia with dystrophic nails on
both hands and leftfoot, adrenal heterotophia in left peritesticular region, pancreatic heterotophia in perisplenic lymphnode, nodular excrescene of spleen, and... |
