[HTML][HTML] Genomic profiles of a hepatoblastoma from a patient with Beckwith-Wiedemann syndrome with uniparental disomy on chromosome 11p15 and germline …

SY Kim, SH Jung, MS Kim, MR Han, HC Park… - Oncotarget, 2017 - ncbi.nlm.nih.gov
Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth disorder mainly
associated with altered genomic imprinting at chromosome 11p15. 5. Children with BWS …

Hepatoblastoma in a child with a paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p causing focal congenital hyperinsulinism

EA Calton, IK Temple, DJG Mackay, M Lever… - European Journal of …, 2013 - Elsevier
Hepatoblastoma is a tumour of early childhood occurring in association with genetic
syndromes including Beckwith–Wiedemann Syndrome (BWS) which results from dominance …

Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith–Wiedemann syndrome

A Mussa, GB Ferrero, B Ceoloni, E Basso… - European journal of …, 2011 - Springer
Beckwith–Wiedemann syndrome is an overgrowth disorder characterized by neonatal
macrosomia, abdominal wall defects, macroglossia, renal anomalies, organomegaly …

Concurrent hepatoblastoma and Wilms tumor leading to diagnosis of Beckwith-Wiedemann syndrome

DM Wolfe, AW Carrion, MM Masukhani… - Journal of pediatric …, 2023 - journals.lww.com
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-associated hepatoblastoma: wnt signal activation occurs later in tumorigenesis in patients with 11p15. 5 uniparental disomy

R Fukuzawa, J Hata, Y Hayashi, H Ikeda… - Pediatric and …, 2003 - Springer
Beckwith-Wiedemann syndrome (BWS) patients with chromosome 11p15. 5 uniparental
isodisomy (UPD) have an increased risk for developing embryonal tumors. UPD in these …

[HTML][HTML] Occurrence of Hepatoblastomas in Patients with Beckwith–Wiedemann Spectrum (BWSp)

SD Klein, M DeMarchis, RL Linn, SP MacFarland… - Cancers, 2023 - mdpi.com
Simple Summary Beckwith–Wiedemann syndrome (BWS) is an overgrowth and cancer
predisposition disorder that is associated with increased risk of hepatoblastoma (HB), a liver …

[PDF][PDF] Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome

NS Sobel Naveh, EM Traxler, KA Duffy… - Hepatology …, 2022 - Wiley Online Library
Abstract Beckwith‐Wiedemann Syndrome (BWS) is the most common human overgrowth
disorder caused by structural and epigenetic changes to chromosome 11p15. Patients with …

Screening hepatoblastoma in Beckwith-Wiedemann syndrome: a complex issue

A Mussa, GB Ferrero - Journal of Pediatric Hematology/Oncology, 2015 - journals.lww.com
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 …

[HTML][HTML] Molecular basis of Beckwith–Wiedemann syndrome spectrum with associated tumors and consequences for clinical practice

T Eggermann, ER Maher, CP Kratz, D Prawitt - Cancers, 2022 - mdpi.com
Simple Summary Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is an inborn
overgrowth disorder caused by molecular alterations in chromosome 11p15. 5. These …

Novel deletion in 11p15. 5 imprinting center region 1 in a patient with Beckwith–Wiedemann syndrome provides insight into distal enhancer regulation and …

N Bachmann, R Crazzolara, F Bohne… - Pediatric Blood & …, 2017 - Wiley Online Library
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 …