We conducted a follow‐up study on 15 patients with Wiedemann‐Beckwith syndrome (WBS)
to further clarify major and minor diagnostic clinical characteristics and long‐term …

OBJECTIVE: To assess intrauterine growth in a series of nine fetuses diagnosed with
Beckwith-Wiedemann syndrome. METHODS: Infants confirmed postnatally to have Beckwith …

We describe 18 individuals from five unrelated families with various manifestations of the
Wiedemann‐Beckwith syndrome. Pedigree analysis was performed on the 5 families and on …

A pair of monozygotic twins discordant for Wiedemann-Beckwith syndrome is described. The
probability of monozygosity is 0.995. This observation suggests that the syndrome is unlikely …

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

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 …

Received in revised version 24 November 1995, accepted for publication 3 May 1996 and
Martinez y Martinez et al.), as well as to show the frequencies of features analyzed in one or …

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 …

We report on a patient with Wiedemann‐Beckwith syndrome (WBS) who developed
abdominal neuroblastoma. Although WBS patients are known to have a higher incidence of …

Monozygotic twins discordant for the Wiedemann‐Beckwith syndrome (WBS) were studied
by cytogenetic and molecular methods to determine if a genetic lesion could be detected in …