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Assisted reproduction techniques and prenatal diagnosis of Beckwith–Wiedemann spectrum presenting with omphalocele

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References

  1. Johnson JP, Beischel L, Schwanke C, Styren K, Crunk A, Schoof J, et al. Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome. J Assist Reprod Genet. 2018;35:985–92. https://doi.org/10.1007/s10815-018-1228-z.

    Article  Google Scholar 

  2. Mussa A, Molinatto C, Cerrato F, Palumbo O, Carella M, Baldassarre G, et al. Assisted reproductive techniques and risk of Beckwith-Wiedemann syndrome. Pediatrics. 2017;140:e20164311.

    Article  PubMed  Google Scholar 

  3. Thorburn MJ, Wright ES, Miller CG, Smith-Read EH. Exomphalos-macroglossia-gigantism syndrome in Jamaican infants. Am J Dis Child. 1970;119:316–21.

    CAS  PubMed  Google Scholar 

  4. Mussa A, Russo S, De Crescenzo A, et al. Prevalence of Beckwith-Wiedemann syndrome in north west of Italy. Am J Med Genet A. 2013;161A:2481–6.

    PubMed  Google Scholar 

  5. Mussa A, Russo S, Larizza L, Riccio A, Ferrero GB. (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: a paradigm for genomic medicine. Clin Genet. 2016;89:403–15.

    Article  CAS  PubMed  Google Scholar 

  6. Mussa A, Russo S, De Crescenzo A, et al. (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome. Eur J Hum Genet. 2016;24:183–90.

    Article  CAS  PubMed  Google Scholar 

  7. Brioude F, Lacoste A, Netchine I, Vazquez MP, Auber F, Audry G, et al. Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance. Horm Res Paediatr. 2013;80:457–65.

    Article  CAS  PubMed  Google Scholar 

  8. Ibrahim A, Kirby G, Hardy C, Dias RP, Tee L, Lim D, et al. Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects. Clin Epigenetics. 2014;6:11.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Tenorio J, Romanelli V, Martin-Trujillo A, Fernández GM, Segovia M, Perandones C, et al. Clinical and molecular analyses of Beckwith-Wiedemann syndrome: comparison between spontaneous conception and assisted reproduction techniques. Am J Med Genet A. 2016;170:2740–9.

    Article  CAS  PubMed  Google Scholar 

  10. Vermeiden JP, Bernardus RE. Are imprinting disorders more prevalent after human in vitro fertilization or intracytoplasmic sperm injection? Fertil Steril. 2013;99:642–51.

    Article  PubMed  Google Scholar 

  11. Wilkins-Haug L, Porter A, Hawley P, Benson CB. Isolated fetal omphalocele, Beckwith-Wiedemann syndrome, and assisted reproductive technologies. Birth Defects Res A Clin Mol Teratol. 2009;85:58–62.

    Article  CAS  PubMed  Google Scholar 

  12. Brioude F, Kalish JM, Mussa A, Foster AC, Bliek J, Ferrero GB, et al. Expert consensus document: clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement. Nat Rev Endocrinol. 2018;14:229–49.

    Article  PubMed  Google Scholar 

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Mussa, A., Carli, D., Cardaropoli, S. et al. Assisted reproduction techniques and prenatal diagnosis of Beckwith–Wiedemann spectrum presenting with omphalocele. J Assist Reprod Genet 35, 1925–1926 (2018). https://doi.org/10.1007/s10815-018-1288-0

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  • DOI: https://doi.org/10.1007/s10815-018-1288-0

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