Literature DB >> 33658067

A Beckwith-Wiedemann syndrome case with de novo 24 Mb duplication of chromosome 11p15.5p14.3.

Huling Jiang1, Zepeng Ping1, Jianguo Wang1, Xiaodan Liu1, Yuxia Jin1, Suping Li1, Chiyan Zhou1, Pinghua Huang1, Yi Jin1, Ling Ai1, Jie Chen2,3.   

Abstract

BACKGROUND: Molecular genetic testing for the 11p15-associated imprinting disorder Beckwith-Wiedemann syndrome (BWS) is challenging because of the molecular heterogeneity and complexity of the affected imprinted regions. An integrated molecular approach to analyze the epigenetic-genetic alterations is required for accurate diagnosis of BWS. CASE
PRESENTATION: We reported a Chinese case with BWS detected by SNP array analysis and methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA). The genetic analysis showed a de novo duplication of 24 Mb at 11p15.5p14.3 is much longer than ever reported. MS-MLPA showed copy number changes with a peak height ratio value of 1.5 (three copies) at 11p15. The duplication of paternal origin with increase of methylation index of 0.68 at H19 and decreased methylation index of 0.37 at KCNQ1OT1.
CONCLUSION: Combined chromosome microarray analysis and methylation profiling provided reliable diagnosis for this paternally derived duplication of BWS. The phenotype associated with 11p15 duplications depends on the size, genetic content, parental inheritance and imprinting status. Identification of these rare duplications is crucial for genetic counselling.

Entities:  

Keywords:  Beckwith-wiedemann syndrome (BWS); Chromosome 11p15.5; Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA); Paternal duplication; Single Nucleotide polymorphism (SNP) array analysis

Year:  2021        PMID: 33658067      PMCID: PMC7931524          DOI: 10.1186/s13039-021-00532-7

Source DB:  PubMed          Journal:  Mol Cytogenet        ISSN: 1755-8166            Impact factor:   2.009


  23 in total

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Authors:  Adam C Smith; Masako Suzuki; Reid Thompson; Sanaa Choufani; Michael J Higgins; Idy W Chiu; Jeremy A Squire; John M Greally; Rosanna Weksberg
Journal:  Genomics       Date:  2011-11-03       Impact factor: 5.736

Review 2.  Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.

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Review 3.  Beckwith-Wiedemann syndrome.

Authors:  Sanaa Choufani; Cheryl Shuman; Rosanna Weksberg
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-08-15       Impact factor: 3.908

4.  Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis.

Authors:  Nadine Bachmann; Roman Crazzolara; Florian Bohne; Dieter Kotzot; Kathrin Maurer; Thorsten Enklaar; Dirk Prawitt; Carsten Bergmann
Journal:  Pediatr Blood Cancer       Date:  2016-09-21       Impact factor: 3.167

5.  Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

Authors:  J L Thorvaldsen; K L Duran; M S Bartolomei
Journal:  Genes Dev       Date:  1998-12-01       Impact factor: 11.361

6.  {beta}-thalassemia major evolution from {beta}-thalassemia minor is associated with paternal uniparental isodisomy of chromosome 11p15.

Authors:  Jan-Gowth Chang; Wen-Chan Tsai; Inn-Wen Chong; Chao-Sung Chang; Chyi-Chang Lin; Ta-Chih Liu
Journal:  Haematologica       Date:  2008-04-15       Impact factor: 9.941

Review 7.  Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.

Authors:  Frédéric Brioude; Jennifer M Kalish; Alessandro Mussa; Alison C Foster; Jet Bliek; Giovanni Battista Ferrero; Susanne E Boonen; Trevor Cole; Robert Baker; Monica Bertoletti; Guido Cocchi; Carole Coze; Maurizio De Pellegrin; Khalid Hussain; Abdulla Ibrahim; Mark D Kilby; Malgorzata Krajewska-Walasek; Christian P Kratz; Edmund J Ladusans; Pablo Lapunzina; Yves Le Bouc; Saskia M Maas; Fiona Macdonald; Katrin Õunap; Licia Peruzzi; Sylvie Rossignol; Silvia Russo; Caroleen Shipster; Agata Skórka; Katrina Tatton-Brown; Jair Tenorio; Chiara Tortora; Karen Grønskov; Irène Netchine; Raoul C Hennekam; Dirk Prawitt; Zeynep Tümer; Thomas Eggermann; Deborah J G Mackay; Andrea Riccio; Eamonn R Maher
Journal:  Nat Rev Endocrinol       Date:  2018-01-29       Impact factor: 43.330

8.  Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours.

Authors:  Y Satoh; H Nakadate; T Nakagawachi; K Higashimoto; K Joh; Z Masaki; J Uozumi; Y Kaneko; T Mukai; H Soejima
Journal:  Br J Cancer       Date:  2006-08-08       Impact factor: 7.640

9.  De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome.

Authors:  Qin Wang; Qian Geng; Qinghua Zhou; Fuwei Luo; Peining Li; Jiansheng Xie
Journal:  Mol Cytogenet       Date:  2017-12-19       Impact factor: 2.009

10.  Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome.

Authors:  Carla Eßinger; Stephanie Karch; Ute Moog; György Fekete; Anna Lengyel; Eva Pinti; Thomas Eggermann; Matthias Begemann
Journal:  Clin Epigenetics       Date:  2020-05-11       Impact factor: 6.551

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