Literature DB >> 30719840

Beckwith-Wiedemann syndrome in diverse populations.

Kelly A Duffy1, Brian J Sajorda1, Alice C Yu1, Evan R Hathaway1, Katheryn L Grand1, Matthew A Deardorff1,2, Jennifer M Kalish1,2,3.   

Abstract

Beckwith-Wiedemann syndrome (BWS) is the most common epigenetic overgrowth disorder and presents with patients affected by a variety of clinical features. Although genotype-phenotype correlations have been demonstrated in BWS and although BWS has been reported to occur equally among racial and ethnic backgrounds, no study to date has evaluated the frequency of findings in different backgrounds. In this study, we evaluated the incidence of clinical features and molecular diagnoses among patients with BWS in Caucasian, Mixed, and non-Caucasian groups. These results suggest that clinical features and molecular diagnoses differ between race/ethnicity groups and raise the possibility of race and ethnicity effects on genotype-phenotype correlations in BWS.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  Beckwith-Wiedemann syndrome; diverse populations; imprinting; methylation; overgrowth; race

Mesh:

Year:  2019        PMID: 30719840      PMCID: PMC6454922          DOI: 10.1002/ajmg.a.61053

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  32 in total

1.  Quantitative analysis of methylation status at 11p15 and 7q21 for the genetic diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome.

Authors:  Beom Hee Lee; Gu-Hwan Kim; Tae Jeong Oh; Joo Hyun Kim; Jin-Joo Lee; Seung Hoon Choi; Joo Yeon Lee; Jae-Min Kim; In Hee Choi; Yoo-Mi Kim; Jin-Ho Choi; Han-Wook Yoo
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2.  Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance.

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Journal:  Horm Res Paediatr       Date:  2013-12-04       Impact factor: 2.852

3.  (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.

Authors:  Alessandro Mussa; Silvia Russo; Agostina De Crescenzo; Andrea Freschi; Luciano Calzari; Silvia Maitz; Marina Macchiaiolo; Cristina Molinatto; Giuseppina Baldassarre; Milena Mariani; Luigi Tarani; Maria Francesca Bedeschi; Donatella Milani; Daniela Melis; Andrea Bartuli; Maria Vittoria Cubellis; Angelo Selicorni; Margherita Cirillo Silengo; Lidia Larizza; Andrea Riccio; Giovanni Battista Ferrero
Journal:  Eur J Hum Genet       Date:  2015-04-22       Impact factor: 4.246

4.  Hyperinsulinism in syndromal disorders.

Authors:  T Meissner; W Rabl; K Mohnike; S Scholl; R Santer; E Mayatepek
Journal:  Acta Paediatr       Date:  2001-08       Impact factor: 2.299

5.  Pancreatic surgery in infants with Beckwith-Wiedemann syndrome and hyperinsulinism.

Authors:  Pablo Laje; Andrew A Palladino; Tricia R Bhatti; Lisa J States; Charles A Stanley; N Scott Adzick
Journal:  J Pediatr Surg       Date:  2013-12       Impact factor: 2.545

6.  Fetal growth patterns in Beckwith-Wiedemann syndrome.

Authors:  A Mussa; S Russo; A de Crescenzo; A Freschi; L Calzari; S Maitz; M Macchiaiolo; C Molinatto; G Baldassarre; M Mariani; L Tarani; M F Bedeschi; D Milani; D Melis; A Bartuli; M V Cubellis; A Selicorni; M C Silengo; L Larizza; A Riccio; G B Ferrero
Journal:  Clin Genet       Date:  2016-03-15       Impact factor: 4.438

Review 7.  [Umbilical hernia in children].

Authors:  Smiljana Marinković; Svetlana Bukarica
Journal:  Med Pregl       Date:  2003 May-Jun

8.  Renal abnormalities in beckwith-wiedemann syndrome are associated with 11p15.5 uniparental disomy.

Authors:  Michael Goldman; Adam Smith; Cheryl Shuman; Oana Caluseriu; Chihong Wei; Leslie Steele; Peter Ray; Paul Sadowski; Jeremy Squire; Rosanna Weksberg; Norman D Rosenblum
Journal:  J Am Soc Nephrol       Date:  2002-08       Impact factor: 10.121

9.  Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith-Wiedemann syndrome.

Authors:  Jennifer M Kalish; Kara E Boodhansingh; Tricia R Bhatti; Arupa Ganguly; Laura K Conlin; Susan A Becker; Stephanie Givler; Lindsey Mighion; Andrew A Palladino; N Scott Adzick; Diva D De León; Charles A Stanley; Matthew A Deardorff
Journal:  J Med Genet       Date:  2015-11-06       Impact factor: 6.318

10.  Frequency of anomalies and hospital outcomes in infants with gastroschisis and omphalocele.

Authors:  Kristin M Corey; Christoph P Hornik; Matthew M Laughon; Kerstin McHutchison; Reese H Clark; P Brian Smith
Journal:  Early Hum Dev       Date:  2014-06-11       Impact factor: 2.699

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  10 in total

1.  Epigenetic Abnormalities of 11p15.5 Region in Beckwith-Wiedemann Syndrome - A Report of Eight Indian Cases.

Authors:  Alec Reginald Errol Correa; Puneeta Mishra; Madhulika Kabra; Neerja Gupta
Journal:  Indian J Pediatr       Date:  2020-01-29       Impact factor: 1.967

2.  Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management.

Authors:  Kelly A Duffy; Kelly L Trout; Jennifer M Gunckle; Shari McCullen Krantz; John Morris; Jennifer M Kalish
Journal:  Front Pediatr       Date:  2021-12-14       Impact factor: 3.418

3.  Phenotypes and epigenetic errors in patients with Beckwith-Wiedemann syndrome in China.

Authors:  Miaoying Zhang; Chengjun Sun; Renchao Liu; Chenbin Dong; Ruoqian Cheng; Zhangqian Zheng; Bingbing Wu; Feihong Luo; Zhou Pei; Wei Lu
Journal:  Transl Pediatr       Date:  2020-10

4.  Maxillo-Facial Morphology in Beckwith-Wiedemann Syndrome: A Preliminary Study on (epi)Genotype-Phenotype Association in Caucasians.

Authors:  Patrizia Defabianis; Alessandro Mussa; Rossella Ninivaggi; Diana Carli; Federica Romano
Journal:  Int J Environ Res Public Health       Date:  2022-02-20       Impact factor: 3.390

5.  The Prevalence of Difficult Airway in Children With Beckwith-Wiedemann Syndrome: A Retrospective Cohort Study.

Authors:  Luis Sequera-Ramos; Kelly A Duffy; John E Fiadjoe; Annery G Garcia-Marcinkiewicz; Bingqing Zhang; Alison Perate; Jennifer M Kalish
Journal:  Anesth Analg       Date:  2021-12-01       Impact factor: 5.108

6.  Clinical and Cytogenomic Characterization of De Novo 11p14.3-p15.5 Duplication Associated with 18q23 Deletion in an Egyptian Female Infant.

Authors:  Hanan H Afifi; Ghada Y El-Kamah; Alaa K Kamel; Sally G Abd Allah; Sayda Hammad; Mohammed M Sayed-Ahmed; Shymaa H Hussein; Amal M Mohamed
Journal:  J Pediatr Genet       Date:  2020-04-21

Review 7.  Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome.

Authors:  Suhee Chang; Marisa S Bartolomei
Journal:  Dis Model Mech       Date:  2020-05-26       Impact factor: 5.758

8.  Clinical and molecular features of children with Beckwith-Wiedemann syndrome in China: a single-center retrospective cohort study.

Authors:  Ruixue Wang; Yongmei Xiao; Dan Li; Hui Hu; Xiaolu Li; Ting Ge; Ronghua Yu; Yizhong Wang; Ting Zhang
Journal:  Ital J Pediatr       Date:  2020-04-29       Impact factor: 2.638

Review 9.  Beckwith-Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature.

Authors:  Hela Sassi; Yasmina Elaribi; Houweyda Jilani; Imen Rejeb; Syrine Hizem; Molka Sebai; Nadia Kasdallah; Habib Bouthour; Samia Hannachi; Jasmin Beygo; Ali Saad; Karin Buiting; Dorra H'mida Ben-Brahim; Lamia BenJemaa
Journal:  Mol Genet Genomic Med       Date:  2021-09-12       Impact factor: 2.183

Review 10.  The influence of social determinants of health on the genetic diagnostic odyssey: who remains undiagnosed, why, and to what effect?

Authors:  Yarden S Fraiman; Monica H Wojcik
Journal:  Pediatr Res       Date:  2020-09-15       Impact factor: 3.756

  10 in total

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