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Retracted

This article has been retracted as the same case report was found to have been presented in the following previously published article: “Achondroplasia with 47, xxy karyotype: A case report of the neonatal diagnosis of an extremely unusual association,” BMC Pediatrics 2012, 12:88. The article has also been published without the consent of Dr. Cristina Martinez-Payo. The first author, Dr. Esther Perez-Carbajo, assumes full responsibility.

View the original article here.

References

  1. E. Perez-Carbajo, I. Zapardiel, L. Sanfrutos-Llorente, S. Cruz-Melguizo, C. Martinez-Payo, and E. Iglesias-Goy, “Prenatal diagnosis of concurrent achondroplasia and klinefelter syndrome,” Case Reports in Obstetrics and Gynecology, vol. 2015, Article ID 980749, 2 pages, 2015.
Case Reports in Obstetrics and Gynecology
Volume 2015 (2015), Article ID 980749, 2 pages
http://dx.doi.org/10.1155/2015/980749
Case Report

Prenatal Diagnosis of Concurrent Achondroplasia and Klinefelter Syndrome

1Obstetrics and Gynecology Department, Puerta de Hierro Majadahonda University Hospital, 28222 Madrid, Spain
2Obstetrics and Gynecology Department, La Paz University Hospital, 28046 Madrid, Spain

Received 6 December 2014; Accepted 5 February 2015

Academic Editor: Giovanni Monni

Copyright © 2015 Esther Perez-Carbajo 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. M. Sendrail, L. Gleizes, M. Sendrail-Pesqué, and P. Colombiés, “Klinefelter's polygonosomy and achondroplasia,” La Semaine des Hopitaux : Organe Fonde par l“Association d”Enseignement Medical des Hopitaux de Paris, vol. 43, no. 18, pp. 1217–1225, 1967. View at Google Scholar · View at Scopus
  2. T. A. Kulakova and I. T. Ignat'ev, “Achondroplasia associated with Klinefelter's syndrome,” Klinicheskaia Meditsina, vol. 64, no. 3, pp. 126–128, 1986. View at Google Scholar · View at Scopus
  3. B. S. Sayli, D. Gul, and H. Cakirbay, “Achondroplasia with XXY karyotype,” Clinical Genetics, vol. 45, pp. 217–218, 1994. View at Google Scholar
  4. A. Juul, L. Aksglaede, A. M. Lund, M. Duno, N. E. Skakkebæk, and E. Rajpert-De Meyts, “Preserved fertility in a non-mosaic Klinefelter patient with a mutation in the fibroblast growth factor receptor 3 gene: case report,” Human Reproduction, vol. 22, no. 7, pp. 1907–1911, 2007. View at Publisher · View at Google Scholar · View at Scopus
  5. E. Maymon, “Anomalías esqueléticas en el feto,” in Ecografia en Ginecologia y Obstetricia, C. Fleischer, F. A. Manning, P. Jeanty, and R. Romero, Eds., pp. 445–506, The McGraw-Hill, New York, NY, USA, 2004. View at Google Scholar
  6. N. J. Sebire, R. J. M. Snijders, R. Brown, T. Southall, and K. H. Nicolaides, “Detection of sex chromosome abnormalities by nuchal translucency screening at 10–14 weeks,” Prenatal Diagnosis, vol. 18, no. 6, pp. 581–584, 1998. View at Publisher · View at Google Scholar