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

被引:68
作者
Mussa, Alessandro [1 ]
Di Candia, Stefania [2 ]
Russo, Silvia [3 ]
Catania, Serena [4 ]
De Pellegrin, Maurizio [5 ]
Di Luzio, Luisa [6 ]
Ferrari, Mario [7 ]
Tortora, Chiara [7 ]
Meazzini, Maria Costanza [7 ]
Brusati, Roberto [7 ]
Milani, Donatella [8 ]
Zampino, Giuseppe [9 ]
Montirosso, Rosario [10 ]
Riccio, Andrea [11 ,12 ]
Selicorni, Angelo [13 ]
Cocchi, Guido [14 ]
Ferrero, Giovanni Battista [1 ]
机构
[1] Univ Turin, Dept Publ Hlth & Pediat Sci, I-10126 Turin, Italy
[2] Ist Sci San Raffaele, Dept Pediat, I-20132 Milan, Italy
[3] Ist Auxol Italiano, Lab Cytogenet & Mol Genet, Milan, Italy
[4] Fdn IRCCS Ist Nazl Tumori, Dept Hematol & Pediat Oncol, Pediat Oncol Unit, Milan, Italy
[5] IRCCS Osped San Raffaele, Pediat Orthopaed Unit, Milan, Italy
[6] Osped Niguarda Ca Granda, Obstet & Gynecol Unit, Milan, Italy
[7] San Paolo Univ Hosp, Reg Ctr CLP, Smile House, Milan, Italy
[8] Univ Milan, Pediat Highly Intens Care Unit, Dept Pathophysiol & Transplantat, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy
[9] Univ Cattolica Sacro Cuore, Ctr Rare Dis, Dept Pediat, Rome, Italy
[10] IRCCS Eugenio Medea, Inst Sci, Ctr Study Social Emot Dev Risk Infant 0 3, Bosisio Parini, Lecco, Italy
[11] Univ Naples 2, DiSTABiF, Naples, Italy
[12] CNR, Inst Genet & Biophys A Buzzati Traverso, I-80125 Naples, Italy
[13] S Gerardo Hosp, MBBM Fdn, Pediat Clin, Clin Pediat Genet Unit, Monza, Italy
[14] Univ Bologna, Alma Mater Studiorum, GC Dept Pediat, Bologna, Italy
关键词
Beckwith-Wiedemann syndrome; Overgrowth; Cancer predisposition; Recommendations; Follow-up; IN-VITRO FERTILIZATION; WILMS-TUMOR; HYPERINSULINEMIC HYPOGLYCEMIA; EPIGENETIC ALTERATIONS; IMPRINTING DISORDERS; TONGUE REDUCTION; CHILDREN; HEPATOBLASTOMA; METHYLATION; RISK;
D O I
10.1016/j.ejmg.2015.11.008
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. (C) 2015 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:52 / 64
页数:13
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