Background We undertook a cost‐benefit analysis of screening for Wilms tumor and
hepatoblastoma in children with Beckwith‐Wiedemann syndrome (BWS), a known cancer …

Abstract Beckwith–Wiedemann Syndrome (BWS) results from mutations or epigenetic
events involving imprinted genes at 11p15. 5. Most BWS cases are sporadic and uniparental …

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

Objective: Beckwith-Wiedemann Syndrome (BWS) is an overgrowth syndrome associated
with macrosomia, omphalocele, macroglossia, visceromegaly and Wilms tumor (WT). We …

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

Literature review and clinical findings in four affected adult males from one family suggest
that there are serious and currently ill‐defined health risks in adults with Beckwith …

Abstract Background Beckwith-Wiedemann syndrome (BWS) is a cancer predisposition
syndrome caused by defects on chromosome 11p15. 5. The quantitative cancer risks in …

Abstract The Beckwith‐Wiedemann syndrome (BWS) is an overgrowth malformation
syndrome that occurs with an incidence of 1: 13,700 births. There is a striking incidence of …

Idiopathic hemihypertrophy (IH) is a congenital overgrowth syndrome associated with an
increased risk of embryonal cancers in childhood. A related developmental disorder is …

Beckwith–Wiedemann syndrome (BWS) is the most common genetic overgrowth syndrome,
and it is frequently clinically recognizable because of characteristic features. These features …