The Beckwith-Wiedemann syndrome is an unusual complex of abnormalities that includes mainly omphalocele, macroglossia, natal and postnatal gigantism, visceromegaly and neonatal hypoglycemia. A case is presented where sonographic prenatal diagnosis of this rare condition was made. Prenatal findings and postnatal management are described.
|Number of pages||6|
|Journal||European Journal of Obstetrics, Gynecology and Reproductive Biology|
|State||Published - 1 Jan 1989|