We report on the prenatal diagnosis of Beckwith‐Wiedemann syndrome (BWS) in a
pregnancy monitored because of a previously affected child. The proposita had classical …

In 1963 Beckwith'presented the necropsy findings of three unrelated children with exompha-
los, macroglossia, hyperplasia of the kidneys and pancreas, and adrenal cytomegaly, and …

In utero diagnosis of Beckwith-Wiedeman syndrome was made after sonographic
identification of an omphalocele and organomegaly in a term fetus. Although not all possible …

Beckwith‐Wiedemann syndrome (BWS) is a congenital overgrowth syndrome with variable
expression. To define the range and frequency of complications in BWS, we have studied a …

Abstract The Beckwith-Wiedemann syndrome is an unusual complex of abnormalities that
includes mainly omphalocele, macroglossia, natal and postnatal gigantism, visceromegaly …

Seven cases of the Beckwith-Wiedemann syndrome are reported. The features of the
syndrome may include macroglossia, omphalocele or umbilical hernia, visceromegaly …

Abstract When Beckwith–Wiedemann syndrome (BWS) is detected prenatally, it is usually
on the basis of macroglossia, exomphalos or enlarged kidneys. We describe a case that …

Abstract Beckwith-Wiedemann syndrome (BWS), though a well-delineated clinical and
morphological entity, can be difficult to diagnose by prenatal ultrasound examination when …

Discussion Beckwith-Wiedemann syndrome is one of the most common congenital
overgrowth syndromes, affecting slightly more than one in 13,700 births. The syndrome was …

A 20‐year‐old woman with Beckwith‐Wiedemann syndrome (BWS) was
ultrasonographically appraised at intervals during her pregnancy. Unequivocal evidence for …