The main features of Wiedemann-Beckwith syndrome (WBS) include macroglossia,
abdominal wall defects, visceromegaly, gigantism, hypoglycemia, ear creases, nevus …

Abstract The Wiedemann-Beckwith syndrome (WBS) comprises an accumulation of multiple
congenital anomalies. Exomphalos, macroglossia and gigantism are considered the most …

In pediatrics and genetics, a great deal of attention has been focused on intrauterine growth
retardation (IUGR), which may occur alone or with a great many anomalies, making up …

Abstract Objectives The diagnosis of Beckwith–Wiedemann syndrome (BWS) typically is
made after birth. To our knowledge, no established guidelines exist for the prenatal …

Pregnancy that results in a child with Beckwith–Wiedemann syndrome (BWS) is associated
with preterm delivery. Based on previous case series, we hypothesized that preterm delivery …

We describe three unrelated cases of Wiedemann‐Beckwith syndrome (WBS). Two of them
were diagnosed postnatally while the third was detected during pregnancy that resulted in …

A previously unreported family in which seven members in two generations have Beckwith-
Wiedemann syndrome (BWS) is documented. Paternal imprinting of the gene responsible …

Introduction eckwith-Wiedemann syndrome (BWS) is a com-mon genetic overgrowth
syndrome that is associated with visceromegaly, macroglossia, ab-dominal wall defects, pre …

We report on 2 patients who were apparently normal at birth but later developed
characteristics of Wiedemann‐Beckwith syndrome (WBS). Both had hypoglycemia …

This book is a catalog of detailed information on approximately 800 conditions that have
been diagnosed prenatally. It includes the methods of detecting fetal abnormalities, the …