| Peer-Reviewed

Current Status of Nursing Research on Beckwith Wiedemann Syndrome Based on Co-word Analysis

Received: 7 November 2019    Accepted: 28 November 2019    Published: 11 December 2019
Views:       Downloads:
Abstract

Using the "Beckwith Wiedemann" "care" or "Beckwith Wiedemann" "nursing" literature in the core collection of Web of Science (WOS) as a data source to understand and analyze the current status of nursing research in Beckwith Wiedemann syndrome for Beckwith Wiedemann syndrome care Provide clinical and research references. The selected literature titles are imported into the literature bibliographic information statistical analysis tool (SATI) to perform frequency statistics on the subject words, matrix is generated, and the results are imported into SPSS 22.0 for drawing cluster analysis and multidimensional scale analysis map. Based on the clustering analysis of high-frequency subject words and the results of multidimensional scaling analysis, the research focus on Beckwith Wiedemann syndrome nursing is: Beckwith Wiedemann syndrome nursing research has experienced a slow development period, and is now in a prosperous period, but the overall number of studies is low. The content coverage is comprehensive but not in-depth and should be improved. The research and exploration of Beckwith Wiedemann syndrome care can be further combined with the current research hotspots to improve the quantity and quality of Beckwith Wiedemann syndrome nursing research.

Published in World Journal of Public Health (Volume 4, Issue 4)
DOI 10.11648/j.wjph.20190404.15
Page(s) 102-108
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Co-word Analysis, Beckwith Wiedemann Syndrome, Research Status, Nursing

References
[1] Brioude F, Netchine I, Praz F, et al. Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization [J]. Human mutation, 2015; 36 (9): 894-902.
[2] Tunster SJ, Van de Pette M, John RM. Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome [J]. Disease models & mechanisms, 2011; 4 (6): 814-821.
[3] Poole RL, Leith DJ, Docherty LE, et al. Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1 [J]. European journal of human genetics: EJHG, 2012; 20 (2): 240-243.
[4] Duquesnes N, Callot C, Jeannot P, et al. p57 (Kip2) knock-in mouse reveals CDK-independent contribution in the development of Beckwith-Wiedemann syndrome [J]. The Journal of pathology, 2016; 239 (3): 250-261.
[5] Gripp KW, Robbins KM, Sheffield BS, et al. Paternal uniparental disomy 11p15.5 in the pancreatic nodule of an infant with Costello syndrome: Shared mechanism for hyperinsulinemic hypoglycemia in neonates with Costello and Beckwith-Wiedemann syndrome and somatic loss of heterozygosity in Costello syndrome driving clonal expansion [J]. American journal of medical genetics Part A, 2016; 170 (3): 559-564.
[6] Ohtsuka Y, Higashimoto K, Sasaki K, et al. Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome [J]. Clinical genetics, 2015; 88 (3): 261-266.
[7] Batra M, Valecha UK. Anesthetic management of tongue reduction in a case of Beckwith-Wiedemann syndrome [J]. Journal of anaesthesiology, clinical pharmacology, 2014; 30 (4): 562-564.
[8] Tunster SJ, Van de Pette M, Creeth HDJ, et al. Fetal growth restriction in a genetic model of sporadic Beckwith-Wiedemann syndrome [J]. Disease models & mechanisms, 2018; 11 (11).
[9] Singh VB, Sribenja S, Wilson KE, et al. Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome [J]. Development (Cambridge, England), 2017; 144 (10): 1820-1830.
[10] Jacob KJ, Robinson WP, Lefebvre L. Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth [J]. Clinical genetics, 2013; 84 (4): 326-334.
[11] White JC, Liu J, Nahar A. Simultaneous Presentation of Wilms Tumor and Immature Ovarian Teratoma in Beckwith-Wiedemann Syndrome [J]. Journal of pediatric hematology/oncology, 2018; 40 (1): e61-e63.
[12] Udayakumaran S, Onyia CU. Beckwith-Wiedemann syndrome and Chiari I malformation--a case-based review of central nervous system involvement in hemihypertrophy syndromes [J]. Child's nervous system: ChNS: official journal of the International Society for Pediatric Neurosurgery, 2015; 31 (5): 637-641.
[13] Knopp C, Rudnik-Schoneborn S, Zerres K, et al. Twenty-one years to the right diagnosis - clinical overlap of Simpson-Golabi-Behmel and Beckwith-Wiedemann syndrome [J]. American journal of medical genetics Part A, 2015; 167a (1): 151-155.
[14] Van Lierde K, Galiwango G, Hodges A, et al. Impact of tongue reduction on overall speech intelligibility, articulation and oromyofunctional behavior in 4 children with Beckwith-Wiedemann syndrome [J]. Folia phoniatrica et logopaedica: official organ of the International Association of Logopedics and Phoniatrics (IALP), 2012; 64 (2): 55-63.
[15] Abi Habib W, Azzi S, Brioude F, et al. Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome [J]. Human molecular genetics, 2014; 23 (21): 5763-5773.
[16] Duffy KA, Cielo CM, Cohen JL, et al. Characterization of the Beckwith-Wiedemann spectrum: Diagnosis and management [J]. American journal of medical genetics Part C, Seminars in medical genetics, 2019.
[17] Wang Q, Geng Q, Zhou Q, et al. De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome [J]. Molecular cytogenetics, 2017; 10: 46.
[18] MacFarland SP, Duffy KA, Bhatti TR, et al. Diagnosis of Beckwith-Wiedemann syndrome in children presenting with Wilms tumor [J]. Pediatric blood & cancer, 2018; 65 (10): e27296.
[19] Kalish JM, Deardorff MA. Tumor screening in Beckwith-Wiedemann syndrome-To screen or not to screen? [J]. American journal of medical genetics Part A, 2016; 170 (9): 2261-2264.
[20] Soussi-Zander C. Beckwith-Wiedemann Syndrome Revisited [J]. Human mutation, 2015; 36 (9): iii.
[21] Russo S, Calzari L, Mussa A, et al. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes [J]. Clinical epigenetics, 2016; 8: 23.
[22] Mussa A, Di Candia S, Russo S, et al. Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome [J]. European journal of medical genetics, 2016; 59 (1): 52-64.
[23] Brioude F, Hennekam R, Bliek J, et al. Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply [J]. European journal of human genetics: EJHG, 2018; 26 (4): 471-472.
[24] Davlin AS, Clarkin CM, Kalish JM. Beckwith-Wiedemann Syndrome: Partnership in the Diagnostic Journey of a Rare Disorder [J]. Pediatrics, 2018; 141 (3).
[25] Cammarata-Scalisi F, Avendano A, Stock F, et al. Beckwith-Wiedemann syndrome: clinical and etiopathogenic aspects of a model genomic imprinting entity [J]. Archivos argentinos de pediatria, 2018; 116 (5): 368-373.
[26] Mussa A, Russo S, De Crescenzo A, et al. Prevalence of Beckwith-Wiedemann syndrome in North West of Italy [J]. American journal of medical genetics Part A, 2013; 161a (10): 2481-2486.
[27] Weksberg R, Shuman C, Beckwith JB. Beckwith-Wiedemann syndrome [J]. European journal of human genetics: EJHG, 2010; 18 (1): 8-14.
[28] Aoki A, Shiozaki A, Sameshima A, et al. Beckwith-Wiedemann syndrome with placental chorangioma due to H19-differentially methylated region hypermethylation: a case report [J]. The journal of obstetrics and gynaecology research, 2011; 37 (12): 1872-1876.
[29] Armes JE, McGown I, Williams M, et al. The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia [J]. Pathology, 2012; 44 (6): 519-527.
Cite This Article
  • APA Style

    Yun Chen, Meng Zhang, Lilan He. (2019). Current Status of Nursing Research on Beckwith Wiedemann Syndrome Based on Co-word Analysis. World Journal of Public Health, 4(4), 102-108. https://doi.org/10.11648/j.wjph.20190404.15

    Copy | Download

    ACS Style

    Yun Chen; Meng Zhang; Lilan He. Current Status of Nursing Research on Beckwith Wiedemann Syndrome Based on Co-word Analysis. World J. Public Health 2019, 4(4), 102-108. doi: 10.11648/j.wjph.20190404.15

    Copy | Download

    AMA Style

    Yun Chen, Meng Zhang, Lilan He. Current Status of Nursing Research on Beckwith Wiedemann Syndrome Based on Co-word Analysis. World J Public Health. 2019;4(4):102-108. doi: 10.11648/j.wjph.20190404.15

    Copy | Download

  • @article{10.11648/j.wjph.20190404.15,
      author = {Yun Chen and Meng Zhang and Lilan He},
      title = {Current Status of Nursing Research on Beckwith Wiedemann Syndrome Based on Co-word Analysis},
      journal = {World Journal of Public Health},
      volume = {4},
      number = {4},
      pages = {102-108},
      doi = {10.11648/j.wjph.20190404.15},
      url = {https://doi.org/10.11648/j.wjph.20190404.15},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.wjph.20190404.15},
      abstract = {Using the "Beckwith Wiedemann" "care" or "Beckwith Wiedemann" "nursing" literature in the core collection of Web of Science (WOS) as a data source to understand and analyze the current status of nursing research in Beckwith Wiedemann syndrome for Beckwith Wiedemann syndrome care Provide clinical and research references. The selected literature titles are imported into the literature bibliographic information statistical analysis tool (SATI) to perform frequency statistics on the subject words, matrix is generated, and the results are imported into SPSS 22.0 for drawing cluster analysis and multidimensional scale analysis map. Based on the clustering analysis of high-frequency subject words and the results of multidimensional scaling analysis, the research focus on Beckwith Wiedemann syndrome nursing is: Beckwith Wiedemann syndrome nursing research has experienced a slow development period, and is now in a prosperous period, but the overall number of studies is low. The content coverage is comprehensive but not in-depth and should be improved. The research and exploration of Beckwith Wiedemann syndrome care can be further combined with the current research hotspots to improve the quantity and quality of Beckwith Wiedemann syndrome nursing research.},
     year = {2019}
    }
    

    Copy | Download

  • TY  - JOUR
    T1  - Current Status of Nursing Research on Beckwith Wiedemann Syndrome Based on Co-word Analysis
    AU  - Yun Chen
    AU  - Meng Zhang
    AU  - Lilan He
    Y1  - 2019/12/11
    PY  - 2019
    N1  - https://doi.org/10.11648/j.wjph.20190404.15
    DO  - 10.11648/j.wjph.20190404.15
    T2  - World Journal of Public Health
    JF  - World Journal of Public Health
    JO  - World Journal of Public Health
    SP  - 102
    EP  - 108
    PB  - Science Publishing Group
    SN  - 2637-6059
    UR  - https://doi.org/10.11648/j.wjph.20190404.15
    AB  - Using the "Beckwith Wiedemann" "care" or "Beckwith Wiedemann" "nursing" literature in the core collection of Web of Science (WOS) as a data source to understand and analyze the current status of nursing research in Beckwith Wiedemann syndrome for Beckwith Wiedemann syndrome care Provide clinical and research references. The selected literature titles are imported into the literature bibliographic information statistical analysis tool (SATI) to perform frequency statistics on the subject words, matrix is generated, and the results are imported into SPSS 22.0 for drawing cluster analysis and multidimensional scale analysis map. Based on the clustering analysis of high-frequency subject words and the results of multidimensional scaling analysis, the research focus on Beckwith Wiedemann syndrome nursing is: Beckwith Wiedemann syndrome nursing research has experienced a slow development period, and is now in a prosperous period, but the overall number of studies is low. The content coverage is comprehensive but not in-depth and should be improved. The research and exploration of Beckwith Wiedemann syndrome care can be further combined with the current research hotspots to improve the quantity and quality of Beckwith Wiedemann syndrome nursing research.
    VL  - 4
    IS  - 4
    ER  - 

    Copy | Download

Author Information
  • Department of Neonatology, The First Affiliated Hospital of Jinan University, Guangzhou, China

  • Department of Neonatology, The First Affiliated Hospital of Jinan University, Guangzhou, China

  • Department of Neonatology, The First Affiliated Hospital of Jinan University, Guangzhou, China

  • Sections