The Beckwith‐Wiedemann syndrome phenotype and the risk of cancer

H Schneid, MP Vazquez, C Vacher… - … : The Official Journal …, 1997 - Wiley Online Library
Beckwith‐Wiedermann syndrome (BWS) comprises of a number of childhood abnormalities,
often associated with one or more tumors. Thirty‐eight patients were investigated to …

Simultaneous occurrence of pancreatoblastoma and neuroblastoma in a newborn with beckwith-wiedemann syndrome

S Sorrentino, M Conte, P Nozza… - Journal of Pediatric …, 2010 - journals.lww.com
Beckwith-Wiedemann syndrome is associated with an increased risk of tumors in the
pediatric age. We report the case of a newborn with Beckwith-Wiedemann syndrome …

[PDF][PDF] Mesenchymal hamartoma of the liver in Beckwith-Wiedemann syndrome: a case report.

SH Yoo, HJ Park, SY Cho, CJ Kim - Journal of Pathology and …, 2002 - jpatholtm.org
Beckwith-Wiedemann syndrome is a well-known overgrowth syndrome associated with the
presence of a wide variety of anomalies and increased risk of cancers. Less frequently …

[HTML][HTML] Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants

LCA Cardoso, A Parra, CR Gil, P Arias, N Gallego… - Cancers, 2022 - mdpi.com
Simple Summary Beckwith–Wiedemann syndrome (BWS) is an overgrowth disorder caused
by imprinting or genetic alterations at the 11p15. 5 locus. BWS is considered a spectrum …

[HTML][HTML] Case Report: A Novel Deletion in the 11p15 Region Causing a Familial Beckwith–Wiedemann Syndrome

J Chen, J Xu, Y Yu, L Sun - Frontiers in Genetics, 2021 - frontiersin.org
Beckwith–Wiedemann syndrome (BWS; OMIM 130650) is a human overgrowth and cancer
susceptibility disorder with a wide clinical spectrum, which cannot be predicted based on …

Molecular genetics of Beckwith-Wiedemann syndrome

M Li, JA Squire, R Weksberg - Current opinion in pediatrics, 1997 - journals.lww.com
Beckwith-Wiedemann syndrome (BWS) is an overgrowth disorder characterized by
developmental anomalies, tissue and organ hyperplasia, and an increased risk of …

[HTML][HTML] Beckwith–Wiedemann syndrome with juvenile fibrous nodules and lobular breast tumors: a case report and review of the literature

Y Sato, Y Watanabe, T Morisaki, S Hayashi… - Surgical Case …, 2024 - Springer
Abstract Background Beckwith–Wiedemann syndrome (BWS) is a genomic imprinting
disorder caused by diverse genetic and/or epigenetic disorders of chromosome 11p15. 5 …

Beckwith-Wiedemann syndrome (BWS) current status of diagnosis and clinical management: summary of the first international consensus statement

M Elbracht, D Prawitt, R Nemetschek, C Kratz… - Klinische …, 2018 - europepmc.org
Beckwith-Wiedemann syndrome (BWS) belongs to the group of imprinting disorders and is
characterized by variable clinical features, including overgrowth, macroglossia, abdominal …

Living donor liver transplantation for hepatoblastoma with Beckwith–Wiedemann syndrome

K Sasaki, M Kasahara, A Fukuda… - Pediatric …, 2010 - Wiley Online Library
Sasaki K, Kasahara M, Fukuda A, Shigeta T, Tanaka H, Nakagawa S, Mitsui K, Harada R,
Nakagawa A. Living donor liver transplantation for hepatoblastoma with Beckwith …

Primary Hepatic Tumors

B Morland, JV Goyet - Diseases of the Liver and Biliary System …, 2008 - Wiley Online Library
© 2008 Blackwell Publishing. ISBN: 978-1-4051-6334-7 for a recessive allele at 11p15. 5 in
two patients with hepatoblastoma, mapping to an area in the region of insulin-like growth …