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

Israel Meizner; Rivka Carmi; Miriam Katz; Vaclav Insler

doi:10.1016/0028-2243(89)90045-2

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

Israel Meizner^*, Rivka Carmi, Miriam Katz, Vaclav Insler

^*Corresponding author for this work

Soroka Medical Center

Research output: Contribution to journal › Article › peer-review

18 Scopus citations

Abstract

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.

Original language	English
Pages (from-to)	259-264
Number of pages	6
Journal	European Journal of Obstetrics and Gynecology and Reproductive Biology
Volume	32
Issue number	3
DOIs	https://doi.org/10.1016/0028-2243(89)90045-2
State	Published - Sep 1989
Externally published	Yes

Keywords

Hypoglycemia
Macroglossia
Omphalocele
Visceromegaly

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10.1016/0028-2243(89)90045-2

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AU - Carmi, Rivka

AU - Katz, Miriam

AU - Insler, Vaclav

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AB - 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.

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KW - Macroglossia

KW - Omphalocele

KW - Visceromegaly

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

Abstract

Keywords

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