Beckwith Wiedemann syndrome

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Beckwith Wiedemann syndrome is a rare congenital anomaly characterized by overgrowth and different patterns of anomalies including mostly omphalocele, macrosomia, macroglossia and placental dysplasia

Reference(s):Kotzot D. Prenatal testing for uniparental disomy: indications and clinical relevance. Ultrasound Obstet Gynecol 2008;31(1):100–5. Review. PubMed PMID: 18059071. Izbizky G, Elias D, Gallo A, Farias P, Sod R. Prenatal diagnosis of fetal bilateral adrenal carcinoma. Ultrasound Obstet Gynecol 2005;26(6):669–71. PubMed PMID: 16254889. Schwärzler P, Bernard JP, Senat MV, Ville Y. Prenatal diagnosis of fetal adrenal masses: differentiation between hemorrhage and solid tumor by color Doppler sonography. Ultrasound Obstet Gynecol 1999;13(5):351–5. PubMed PMID: 10380301. Jauniaux E, Nicolaides KH. Early ultrasound diagnosis and follow-up of molar pregnancies. Ultrasound Obstet Gynecol 1997;9(1):17–21. PubMed PMID: 9060124.