Literature DB >> 26592461

Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome.

Alessandro Mussa1, Stefania Di Candia2, Silvia Russo3, Serena Catania4, Maurizio De Pellegrin5, Luisa Di Luzio6, Mario Ferrari7, Chiara Tortora7, Maria Costanza Meazzini7, Roberto Brusati7, Donatella Milani8, Giuseppe Zampino9, Rosario Montirosso10, Andrea Riccio11, Angelo Selicorni12, Guido Cocchi13, Giovanni Battista Ferrero14.   

Abstract

UNLABELLED: Beckwith-Wiedemann syndrome (BWS) is the most common (epi)genetic overgrowth-cancer predisposition disorder. Given the absence of consensual recommendations or international guidelines, the Scientific Committee of the Italian BWS Association (www.aibws.org) proposed these recommendations for the diagnosis, molecular testing, clinical management, follow-up and tumor surveillance of patients with BWS. The recommendations are intended to allow a timely and appropriate diagnosis of the disorder, to assist patients and their families, to provide clinicians and caregivers optimal strategies for an adequate and satisfactory care, aiming also at standardizing clinical practice as a national uniform approach. They also highlight the direction of future research studies in this setting. With recent advances in understanding the disease (epi)genetic mechanisms and in describing large cohorts of BWS patients, the natural history of the disease will be dissected. In the era of personalized medicine, the emergence of specific (epi)genotype-phenotype correlations in BWS will likely lead to differentiated follow-up approaches for the molecular subgroups, to the development of novel tools to evaluate the likelihood of cancer development and to the refinement and optimization of current tumor screening strategies.
CONCLUSIONS: In this article, we provide the first comprehensive recommendations on the complex management of patients with Beckwith-Wiedemann syndrome.
Copyright © 2015 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Beckwith–Wiedemann syndrome; Cancer predisposition; Follow-up; Overgrowth; Recommendations

Mesh:

Year:  2015        PMID: 26592461     DOI: 10.1016/j.ejmg.2015.11.008

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  29 in total

1.  Development of the Serum α-Fetoprotein Reference Range in Patients with Beckwith-Wiedemann Spectrum.

Authors:  Kelly A Duffy; Jennifer L Cohen; Okan U Elci; Jennifer M Kalish
Journal:  J Pediatr       Date:  2019-06-22       Impact factor: 4.406

2.  Beckwith-Wiedemann syndrome in diverse populations.

Authors:  Kelly A Duffy; Brian J Sajorda; Alice C Yu; Evan R Hathaway; Katheryn L Grand; Matthew A Deardorff; Jennifer M Kalish
Journal:  Am J Med Genet A       Date:  2019-02-04       Impact factor: 2.802

3.  Tumor Screening in Beckwith-Wiedemann Syndrome: Parental Perspectives.

Authors:  Kelly A Duffy; Katheryn L Grand; Kristin Zelley; Jennifer M Kalish
Journal:  J Genet Couns       Date:  2017-12-04       Impact factor: 2.537

Review 4.  Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology.

Authors:  Katrin Õunap
Journal:  Mol Syndromol       Date:  2016-07-06

5.  Beckwith-Wiedemann Syndrome: Partnership in the Diagnostic Journey of a Rare Disorder.

Authors:  Alisha S Davlin; Catherine M Clarkin; Jennifer M Kalish
Journal:  Pediatrics       Date:  2018-02-02       Impact factor: 7.124

6.  Obstructive Sleep Apnea in Children With Beckwith-Wiedemann Syndrome.

Authors:  Christopher M Cielo; Kelly A Duffy; Jesse A Taylor; Carole L Marcus; Jennifer M Kalish
Journal:  J Clin Sleep Med       Date:  2019-03-15       Impact factor: 4.062

7.  Wilms tumour in Beckwith-Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines.

Authors:  Jack Brzezinski; Cheryl Shuman; Sanaa Choufani; Peter Ray; Dmitiri J Stavropoulos; Raveen Basran; Leslie Steele; Nicole Parkinson; Ronald Grant; Paul Thorner; Armando Lorenzo; Rosanna Weksberg
Journal:  Eur J Hum Genet       Date:  2017-07-12       Impact factor: 4.246

Review 8.  Obstructive sleep apnoea and the role of tongue reduction surgery in children with Beckwith-Wiedemann syndrome.

Authors:  Christopher M Cielo; Kelly A Duffy; Aesha Vyas; Jesse A Taylor; Jennifer M Kalish
Journal:  Paediatr Respir Rev       Date:  2017-02-24       Impact factor: 2.726

9.  Defining an optimal time window to screen for hepatoblastoma in children with Beckwith-Wiedemann syndrome.

Authors:  Alessandro Mussa; Kelly A Duffy; Diana Carli; Giovanni Battista Ferrero; Jennifer M Kalish
Journal:  Pediatr Blood Cancer       Date:  2018-09-30       Impact factor: 3.167

10.  Urological Findings in Beckwith-Wiedemann Syndrome With Chromosomal Duplications of 11p15.5: Evaluation and Management.

Authors:  Carmen C Tong; Kelly A Duffy; David I Chu; Dana A Weiss; Arun K Srinivasan; Douglas A Canning; Jennifer M Kalish
Journal:  Urology       Date:  2016-09-07       Impact factor: 2.649

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