[HTML][HTML] Investigation of 11p15. 5 Methylation Defects Associated with Beckwith-Wiedemann Spectrum and Embryonic Tumor Risk in Lateralized Overgrowth Patients
B Tüysüz, S Bozlak, D Uludağ Alkaya, S Ocak, B Kasap… - Cancers, 2023 - mdpi.com
Simple Summary Lateralized overgrowth may be isolated or accompany syndromes.
Recently, international BWS consensus proposed that the patients with isolated lateralized …
Recently, international BWS consensus proposed that the patients with isolated lateralized …
Isolated‐and Beckwith‐Wiedemann syndrome related‐lateralised overgrowth (hemihypertrophy): Clinical and molecular correlations in 94 individuals
JA Radley, M Connolly, A Sabir, F Kanani… - Clinical …, 2021 - Wiley Online Library
The congenital imprinting disorder, Beckwith‐Wiedemann syndrome (BWS) is associated
with variable clinical features including hemihypertrophy/lateralised overgrowth (LO) and …
with variable clinical features including hemihypertrophy/lateralised overgrowth (LO) and …
Characterization of the Beckwith‐Wiedemann spectrum: Diagnosis and management
KA Duffy, CM Cielo, JL Cohen… - American Journal of …, 2019 - Wiley Online Library
Beckwith‐Wiedemann syndrome (BWS) is the most common epigenetic overgrowth and
cancer predisposition disorder. Due to both varying molecular defects involving …
cancer predisposition disorder. Due to both varying molecular defects involving …
[HTML][HTML] Characterization and childhood tumor risk assessment of genetic and epigenetic syndromes associated with lateralized overgrowth
JR Griff, KA Duffy, JM Kalish - Frontiers in pediatrics, 2020 - frontiersin.org
Lateralized overgrowth (LO), or segmental overgrowth, is defined as an increase in growth
of tissue (bone, muscle, connective tissue, vasculature, etc.) in any region of the body. Some …
of tissue (bone, muscle, connective tissue, vasculature, etc.) in any region of the body. Some …
[HTML][HTML] 11p15 Epimutations in Pediatric Embryonic Tumors: Insights from a Methylome Analysis
Simple Summary Epigenetics encompasses changes in DNA without changing the DNA
sequence itself, and it includes, among other modifications, DNA methylation. DNA …
sequence itself, and it includes, among other modifications, DNA methylation. DNA …
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous …
S Azzi, S Rossignol, V Steunou, T Sas… - Human molecular …, 2009 - academic.oup.com
Genomic imprinting plays an important role in mammalian development. Loss of imprinting
(LOI) through loss (LOM) or gain (GOM) of methylation is involved in many human disorders …
(LOI) through loss (LOM) or gain (GOM) of methylation is involved in many human disorders …
Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature
H Sassi, Y Elaribi, H Jilani, I Rejeb… - … Genetics & Genomic …, 2021 - Wiley Online Library
Abstract Background Beckwith–Wiedemann syndrome (BWS) is a rare overgrowth
syndrome characterized by congenital malformations and predisposition to embryonic …
syndrome characterized by congenital malformations and predisposition to embryonic …
Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance
F Brioude, A Lacoste, I Netchine, MP Vazquez… - Hormone research in …, 2014 - karger.com
Background: Beckwith-Wiedemann syndrome (BWS) is an overgrowth syndrome associated
with an increased risk of pediatric tumors. The underlying molecular abnormalities may be …
with an increased risk of pediatric tumors. The underlying molecular abnormalities may be …
Cancer risk in Beckwith-Wiedemann syndrome: a systematic review and meta-analysis outlining a novel (Epi) genotype specific histotype targeted screening protocol
A Mussa, C Molinatto, G Baldassarre, E Riberi… - The Journal of …, 2016 - Elsevier
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 …
subgroups: Imprinting Control Region 1 Gain of Methylation (ICR1-GoM), Imprinting Control …
[HTML][HTML] Wilms tumour in Beckwith–Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines
J Brzezinski, C Shuman, S Choufani, P Ray… - European Journal of …, 2017 - nature.com
Abstract Beckwith–Wiedemann Syndrome (BWS) is an overgrowth syndrome caused by a
variety of molecular changes on chromosome 11p15. 5. Children with BWS have a …
variety of molecular changes on chromosome 11p15. 5. Children with BWS have a …
相关搜索
- tumor risk beckwith wiedemann
- tumor risk overgrowth patients
- overgrowth patients beckwith wiedemann
- overgrowth patients methylation defects
- tumor risk methylation defects
- beckwith wiedemann methylation defects
- beckwith wiedemann growth pattern
- loss of methylation wiedemann syndrome
- tumor risk growth pattern
- tunisian patients wiedemann syndrome
- patients with beckwith high frequency
- tumor risk molecular mechanism
- beckwith wiedemann molecular mechanism
- beckwith wiedemann diagnosis and management
- patients with beckwith copy number variations
- beckwith wiedemann screening protocol