[HTML][HTML] Preclinical and clinical epigenetic-based reconsideration of Beckwith-Wiedemann Syndrome

C Papulino, U Chianese, MM Nicoletti… - Frontiers in …, 2020 - frontiersin.org
Epigenetics has achieved a profound impact in the biomedical field, providing new
experimental opportunities and innovative therapeutic strategies to face a plethora of …

Management of adrenal masses in patients with Beckwith–Wiedemann syndrome

SP MacFarland, S Mostoufi‐Moab… - Pediatric blood & …, 2017 - Wiley Online Library
Beckwith–Wiedemann syndrome (BWS) is a genetic overgrowth and cancer predisposition
syndrome, associated with both benign and malignant adrenal findings. Literature review …

[HTML][HTML] Hereditary conditions associated with elevated cancer risk in childhood

EN Suspitsin, EN Imyanitov - Biochemistry (Moscow), 2023 - Springer
Widespread use of the next-generation sequencing (NGS) technologies revealed that a
significant percentage of tumors in children develop as a part of monogenic hereditary …

Genetic Predisposition to Sarcoma: What Should Clinicians Know?

J Vagher, CJ Mehrhoff, V Florou, LD Maese - Current Treatment Options in …, 2024 - Springer
Cancer predisposition syndromes (CPS) are known to cause a variety of sarcomas.
Consideration for genetic testing in patients with a strong family history of cancer, multiple …

A novel tissue‐based ß‐catenin gene and immunohistochemical analysis to exclude familial adenomatous polyposis among children with hepatoblastoma tumors

HJ Dubbink, IHIM Hollink… - Pediatric Blood & …, 2018 - Wiley Online Library
Abstract Background The Wnt/β‐catenin pathway plays a central role in the pathogenesis of
most hepatoblastomas (HBs), that is, up to 60–80% carry activating CTNNB1 mutations. HBs …

Tumor screening in Beckwith-Wiedemann syndrome: parental perspectives

KA Duffy, KL Grand, K Zelley, JM Kalish - Journal of genetic counseling, 2018 - Springer
Abstract Children with Beckwith-Wiedemann Syndrome (BWS) and Isolated
Hemihypertrophy (IHH) are at an increased risk for developing tumors. Tumor screening in …

[HTML][HTML] The potential key genes and pathways associated with Wilms tumor in quest of proper candidates for diagnostic and therapeutic purposes

M Bitaraf, M Mahmanzar, N Zafari… - Scientific Reports, 2022 - nature.com
To designate the probable most important differentially expressed genes and genetic
pathways in Wilms tumor and assess their expression and diagnostic potential by RT-PCR …

[HTML][HTML] Case report of congenital hepatoblastoma with the onset at 30-weeks' gestation

Z Yan, W Bai, L Li, S Li, Y Hua, X Zhang… - Frontiers in Pediatrics, 2022 - frontiersin.org
This study reports a case of hepatoblastoma with onset at 30-weeks' gestation and rapid
growth rate. The postnatal enhanced CT confirmed an intrahepatic mass with a size of 8.5 …

Investigation of (epi) genotype causes and follow‐up manifestations in the patients with classical and atypical phenotype of Beckwith‐Wiedemann spectrum

B Tüysüz, N Güneş, F Geyik, G Yeşil… - American Journal of …, 2021 - Wiley Online Library
Beckwith‐Wiedemann syndrome (BWS) is a genomic imprinting disorder, characterized by
macroglossia, abdominal wall defects, lateralized overgrowth, and predisposition to …

The prevalence of difficult airway in children with Beckwith-Wiedemann syndrome: A retrospective cohort study

L Sequera-Ramos, KA Duffy, JE Fiadjoe… - Anesthesia & …, 2021 - journals.lww.com
BACKGROUND: Beckwith-Wiedemann syndrome (BWS) is the most common congenital
overgrowth disorder with an incidence of approximately 1 in 10,000 live births. The condition …