Diagnóstico pré-natal da síndrome de Beckwith-Wiedemann pela ultrassonografia bidimensional e tridimensional

AUTOR(ES)

Araujo Júnior, Edward, Simioni, Christiane, Nardozza, Luciano Marcondes Machado, Moron, Antonio Fernandes

FONTE

Radiol Bras

DATA DE PUBLICAÇÃO

2013-12

RESUMO

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.

ASSUNTO(S)

diagnóstico pré-natal síndrome de beckwith-wiedemann ultrassonografia bidimensional ultrassonografia tridimensional

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