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Case Reports in Obstetrics and Gynecology
Volume 2014, Article ID 495702, 4 pages
http://dx.doi.org/10.1155/2014/495702
Case Report

Prenatal Diagnosis of a Fetus with Ring Chromosomal 15 by Two- and Three-Dimensional Ultrasonography

1Department of Obstetrics and Gynecology, Medical College Science of Santa Casa of São Paulo (FCMSCSP), 01221-020 São Paulo, SP, Brazil
2Department of Obstetrics, Federal University of São Paulo (UNIFESP), Rua Carlos Weber 956, Apartamento 113 Visage, 05303-000 São Paulo, SP, Brazil
3Department of Gynecology and Obstetrics, Baylor College of Medicine and Texas Children’s Hospital, Houston, TX, USA
4Department of Genetics, Federal University of São Paulo (UNIFESP), 77030 São Paulo, SP, Brazil

Received 29 June 2014; Revised 4 October 2014; Accepted 5 October 2014; Published 20 October 2014

Academic Editor: Eliezer Shalev

Copyright © 2014 Ingrid Schwach Werneck Britto et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. E. Manolakos, A. Vetro, S. Kitmirides et al., “Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH,” Prenatal Diagnosis, vol. 29, no. 9, pp. 884–888, 2009. View at Publisher · View at Google Scholar · View at Scopus
  2. G. Kosztolányi, “Decreased cell viability of fibroblasts from two patients with a ring chromosome: an in vitro reflection of growth failure?” American Journal of Medical Genetics, vol. 28, pp. 181–184, 1987. View at Google Scholar
  3. J. P. Fryns, M. Borghgraef, A. Kleczkowska, and H. van den Berghe, “Ring chromosome 15: follow-up data on physical and psychological development,” Genetic Counseling, vol. 1, no. 2, pp. 167–172, 1990. View at Google Scholar · View at Scopus
  4. M. Kitatani, H. Takahashi, M. Ozaki, E. Okino, and T. Maruoka, “A case of ring chromosome 15 accompanied by almost normal intelligence,” Human Genetics, vol. 85, no. 1, pp. 138–139, 1990. View at Google Scholar · View at Scopus
  5. G. Kosztolányi, “Does “ring syndrome” exist? An analysis of 207 case reports on patients with a ring autosome,” Human Genetics, vol. 75, no. 2, pp. 174–179, 1987. View at Publisher · View at Google Scholar · View at Scopus
  6. Z. Túmer, T. L. Harboe, E. Blennow, V. M. Kalscheuer, N. Tommerup, and K. Brøndum-Nielsen, “Molecular cytogenetic characterization of ring chromosome 15 in three unrelated patients,” American Journal of Medical Genetics, vol. 130, no. 4, pp. 340–344, 2004. View at Publisher · View at Google Scholar · View at Scopus
  7. G. Kosztolányi, K. Méhes, and E. B. Hook, “Inherited ring chromosomes: an analysis of published cases,” Human Genetics, vol. 87, no. 3, pp. 320–324, 1991. View at Publisher · View at Google Scholar · View at Scopus
  8. M. G. Butler, A. B. Fogo, D. A. Fuchs, F. S. Collins, V. G. Dev, and J. A. Phillips III, “Brief clinical report and review: two patients with ring chromosome 15 syndrome,” American Journal of Medical Genetics, vol. 29, no. 1, pp. 149–154, 1988. View at Publisher · View at Google Scholar · View at Scopus
  9. I. A. Glass, K. A. Rauen, E. Chen et al., “Ring chromosome 15: characterization by array CGH,” Human Genetics, vol. 118, no. 5, pp. 611–617, 2006. View at Publisher · View at Google Scholar · View at Scopus
  10. E. Rossi, J. Messa, and O. Zuffardi, “Ring syndrome: still true?” Journal of Medical Genetics, vol. 45, no. 11, pp. 766–768, 2008. View at Publisher · View at Google Scholar · View at Scopus
  11. Y.-H. Liu, S. D. Chang, and F.-P. Chen, “Increased fetal nuchal fold leading to prenatal diagnosis of ring chromosome 15,” Prenatal Diagnosis, vol. 21, no. 12, pp. 1031–1033, 2001. View at Publisher · View at Google Scholar · View at Scopus
  12. E. Hatem, B. R. Meriam, D. Walid, M. Adenen, G. Moez, and S. Ali, “Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia,” Prenatal Diagnosis, vol. 27, no. 5, pp. 471–474, 2007. View at Publisher · View at Google Scholar · View at Scopus
  13. M. Klaassens, M. Van Dooren, H. J. Eussen et al., “Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization,” The American Journal of Human Genetics, vol. 76, no. 5, pp. 877–882, 2005. View at Publisher · View at Google Scholar · View at Scopus
  14. M. Klaassens, R. J. Galjaard, D. A. Scott et al., “Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: two patients and review of the literature,” The American Journal of Medical Genetics. Part A, vol. 143, no. 18, pp. 2204–2212, 2007. View at Google Scholar · View at Scopus
  15. C. P. Chen, C. C. Lee, C. W. Pan, T. Y. Kir, and B. F. Chen, “Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, urinary tract anomalies, congenital heart defect and kyphoscoliosis,” Prenatal Diagnosis, vol. 18, pp. 1289–1293, 1998. View at Google Scholar
  16. D. Schlembach, M. Zenker, U. Trautmann, R. Ulmer, and E. Beinder, “Deletion 15q24-26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic development,” Prenatal Diagnosis, vol. 21, no. 4, pp. 289–292, 2001. View at Publisher · View at Google Scholar · View at Scopus
  17. J. R. Biggio Jr., M. D. Descartes, A. J. Carroll, and R. L. Holt, “Congenital diaphragmatic hernia: is 15q26.1-26.2 a candidate locus?” American Journal of Medical Genetics, vol. 126, no. 2, pp. 183–185, 2004. View at Google Scholar · View at Scopus
  18. I. López, J. A. Bafalliu, M. C. Bernabé, F. García, M. Costa, and E. Guillén-Navarro, “Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects,” Prenatal Diagnosis, vol. 26, no. 6, pp. 577–580, 2006. View at Publisher · View at Google Scholar · View at Scopus