Objective To compare tumor risk in the 4 Beckwith-Wiedemann syndrome (BWS) molecular
subgroups: Imprinting Control Region 1 Gain of Methylation (ICR1-GoM), Imprinting Control …

Simple Summary Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is an inborn
overgrowth disorder caused by molecular alterations in chromosome 11p15. 5. These …

Abstract Patients with Beckwith-Wiedemann syndrome (BWS) are known to be at an
increased risk for childhood malignancies, particularly Wilms tumor and hepatoblastoma …

Beckwith–Wiedemann Spectrum (BWSp) is the most common epigenetic childhood cancer
predisposition disorder. BWSp is caused by (epi) genetic changes affecting the BWS critical …

Abstract Background Beckwith‐Wiedemann syndrome (BWS) phenotype usually mitigates
with age and data on adulthood are limited. Our study aims at reporting phenotype evolution …

Abstract Patients with Beckwith-Wiedemann Syndrome (BWS) are predisposed to
developing hepatoblastoma. Clinical data were reviewed in all cases of hepatoblastoma in …

Conditions like Beckwith-Wiedemann syndrome (BWS) carry a risk of an associated
aggressive malignancy, and thus timely diagnosis is critical. Without a clear diagnosis and …

An infant with persistent hyperinsulinemic hypoglycemia, diffuse nesidioblastosis, and mixed
hamartoma of the liver (MHL), in addition to demonstrating clinical, pathologic, and …

Beckwith–Wiedemann syndrome (BWS) is a genetic imprinting disorder that most commonly
presents as overgrowth, macroglossia, abdominal wall defects, lateralized overgrowth, and …

To determine the incidence and relative risk (RR) of cancer in children with Beckwith-
Wiedemann syndrome (BWS), children with BWS were followed up from birth until death …