Simple Summary Beckwith–Wiedemann syndrome (BWS) is an overgrowth and cancer
predisposition disorder that is associated with increased risk of hepatoblastoma (HB), a liver …

Patients with Beckwith–Wiedemann syndrome (BWS) have an increased risk to develop
cancer in childhood, especially Wilms tumor and hepatoblastoma. The risk varies depending …

Abstract Beckwith‐Wiedemann Syndrome (BWS) is the most common human overgrowth
disorder caused by structural and epigenetic changes to chromosome 11p15. Patients with …

Trobaugh-Lotrario et al 1 are to be congratulated on their detailed review of cases of
Beckwith-Wiedemann Syndrome (BWS) with hepatoblastoma. We think that details …

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

Beckwith-Wiedemann syndrome (BWS) is an epigenetic overgrowth disorder and cancer
predisposition syndrome caused by imprinting defects of chromosome 11p15. 5-11p15. 4 …

Beckwith–Wiedemann syndrome (BWS) is one of the most common cancer predisposition
disorders. As a result, BWS patients receive tumor screening as part of their clinical …

Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth disorder mainly
associated with altered genomic imprinting at chromosome 11p15. 5. Children with BWS …

Beckwith–Wiedemann syndrome (BWS) is a genetic syndrome associated with overgrowth
and cancer predisposition, including predisposition to Wilms tumor (WT). Patients with BWS …

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 …