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

Abstract The Beckwith-Wiedemann syndrome is a cancer predisposition syndrome
characterized by a predilection to embryonal tumor growth, especially Wilms tumor …

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 …

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

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

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 Background Beckwith–Wiedemann syndrome (BWS) is an early‐onset overgrowth
disorder with a high risk for embryonal tumors. It is mainly caused by dysregulation of …

Beckwith–Wiedemann syndrome is an overgrowth disorder characterized by neonatal
macrosomia, abdominal wall defects, macroglossia, renal anomalies, organomegaly …

Beckwith‐Wiedemann syndrome (BWS) is an overgrowth syndrome associated with a
predisposition to embryonal tumors, most commonly Wilms'(WT). Overlapping clinical …

Beckwith-Wiedemann syndrome (BWS) patients with chromosome 11p15. 5 uniparental
isodisomy (UPD) have an increased risk for developing embryonal tumors. UPD in these …