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In utero prenatal diagnosis of Beckwith-Wiedemann syndrome; a case report

✍ Scribed by Meizner, Israel; Carmi, Rivka; Katz, Miriam; Insler, Vaclav

Book ID: 122943029
Publisher: Elsevier Science
Year: 1989
Tongue: English
Weight: 359 KB
Volume: 32
Category: Article
ISSN: 0301-2115
DOI: 10.1016/0028-2243(89)90045-2

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## Abstract Beckwith‐Wiedemann syndrome is an inherited disorder most commonly characterized by prenatal or postnatal overgrowth, macroglossia, omphalocele, unusual earlobe creases, and increased risk of neoplasia. Several reported cases of this syndrome have been prenatally diagnosed, but no repor