Abstract Children with Beckwith–Wiedemann syndrome (BWS) have increased risk for
development of embryonal tumors. We present the case of an infant with BWS who has …

Beckwith–Wiedemann syndrome (BWS) is a genetic disorder associated with an increased
risk of childhood tumors. Here we describe a patient with BWS who developed a central …

Beckwith–Wiedemann syndrome (BWS) is the most common epigenetic overgrowth disorder
and presents with patients affected by a variety of clinical features. Although genotype …

Abstract Beckwith–Wiedemann syndrome (BWS), an overgrowth disorder with several
congenital abnormalities, encompasses nephrourological anomalies. The objective of the …

Genomic imprinting is a rare form of gene expression in mammals in which a small number
of genes are expressed in a parent-of-origin-specific manner. The aetiology of human …

An elevated risk of hepatoblastoma for children with Beckwith-Wiedemann syndrome or
isolated hemihyperplasia is well established. We describe five children with Beckwith …

A number of genetic syndromes have been linked to increased risk for Wilms tumor (WT),
hepatoblastoma (HB), and other embryonal tumors. Here, we outline these rare syndromes …

A 3-month-old Chinese male infant with typical manifestations of Beckwith-Wiedemann
Syndrome (BWS), such as macroglossia, hepatomegaly, umbilical hernia and …

Abstract Background Beckwith-Wiedemann syndrome (BWS), a congenital overgrowth
disorder with variable expressivity and a predisposition to tumorigenesis, results from …

Background Beckwith Wiedemann syndrome (BWS) is an overgrowth condition associated
with a predisposition to develop childhood tumors. BWS is highly variable in clinical …