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

Beckwith-Wiedemann syndrome (BWS) is a growth disorder variably characterized by
neonatal hypoglycemia, macrosomia, macroglossia, hemihyperplasia, omphalocele …

Beckwith–Wiedemann syndrome (BWS) is an imprinting disorder characterized by
overgrowth, tumor predisposition, and congenital malformations. Approximately 85% of …

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 …

Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome with variable
expression. The major features are anterior abdominal wall defects, macroglossia, and …

ABSTRACT Although Beckwith–Wiedemann syndrome (BWS, OMIM# 130650) is the most
common genetic overgrowth disorder, data on its epidemiology are scanty and the estimates …

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 …

Beckwith–Wiedemann syndrome (BWS) is a congenital overgrowth condition with an
increased risk of developing embryonic tumours, such as Wilms' tumour. The cardinal …

Macroglossia, prenatal or postnatal overgrowth, and abdominal wall defects (omphalocele,
umbilical hernia, or diastasis recti) permit early recognition of Beckwith-Wiedemann …