2013
DOI: 10.1590/s0100-39842013000600012
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Prenatal diagnosis of Beckwith-Wiedemann syndrome by two- and three-dimensional ultrasonography

Abstract: Beckwith-Wiedemann syndrome is a genetic syndrome characterized by macroglossia, omphalocele, fetal gigantism and neonatal hypoglycemia. The authors report a case of Beckwith-Wiedemann syndrome diagnosed in a 32-year-old primigravida in whom two-dimensional ultrasonography revealed the presence of abdominal wall cyst, macroglossia and polycystic kidneys. Three-dimensional ultrasonography in rendering mode was of great importance to confirm the previous two-dimensional ultrasonography findings.

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Cited by 6 publications
(1 citation statement)
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“…The ultrasound modality allows a faster scan of the fetus, the image being automatically transformed into a virtual 3D image on the screen (21,23) . Up to the 18th week of gestation, ultrasound allows complete viewing of the fetal body.…”
Section: Discussionmentioning
confidence: 99%
“…The ultrasound modality allows a faster scan of the fetus, the image being automatically transformed into a virtual 3D image on the screen (21,23) . Up to the 18th week of gestation, ultrasound allows complete viewing of the fetal body.…”
Section: Discussionmentioning
confidence: 99%