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Case Reports in Genetics
Volume 2015, Article ID 950574, 4 pages
http://dx.doi.org/10.1155/2015/950574
Case Report

Cognitive, Affective Problems and Renal Cross Ectopy in a Patient with 48,XXYY/47,XYY Syndrome

1Department of Urology, Kahramanmaras Sutcu Imam University, Kahramanmaras, Turkey
2Department of Urology, Nizip State Hospital, Gaziantep, Turkey
3Department of Psychiatry, Kahramanmaras State Hospital, Kahramanmaras, Turkey
4Department of Urology, Adiyaman University, Adiyaman, Turkey

Received 10 March 2015; Accepted 27 April 2015

Academic Editor: Philip D. Cotter

Copyright © 2015 Sefa Resim 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. G. Linden, B. G. Bender, and A. Robinson, “Sex chromosome tetrasomy and pentasomy,” Pediatrics, vol. 96, no. 4, part 1, pp. 672–682, 1995. View at Google Scholar · View at Scopus
  2. J. Visootsak and J. M. Graham Jr., “Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY,” Developmental Disabilities Research Reviews, vol. 15, no. 4, pp. 328–332, 2009. View at Publisher · View at Google Scholar · View at Scopus
  3. J. Visootsak, B. Rosner, E. Dykens, N. Tartaglia, and J. M. Graham Jr., “Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXY,” American Journal of Medical Genetics, Part A, vol. 143, no. 11, pp. 1198–1203, 2007. View at Publisher · View at Google Scholar · View at Scopus
  4. R. Q. Pasqualini, G. Vidal, and G. E. Bur, “Psychopathology of Klinefelter's syndrome; review of thirtyone cases,” The Lancet, vol. 270, no. 6987, pp. 164–167, 1957. View at Publisher · View at Google Scholar · View at Scopus
  5. P. Katulanda, J. R. Rajapakse, J. Kariyawasam, R. Jayasekara, and V. W. Dissanayake, “An adolescent with 48,xxyy syndrome with hypergonadotrophic hypogonadism, attention deficit hyperactive disorder and renal malformations,” Indian Journal of Endocrinology and Metabolism, vol. 16, no. 5, pp. 824–826, 2012. View at Publisher · View at Google Scholar
  6. A. L. Gropman, A. Rogol, I. Fennoy et al., “Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome,” American Journal of Medical Genetics, Part A, vol. 152, no. 6, pp. 1523–1530, 2010. View at Publisher · View at Google Scholar · View at Scopus
  7. C. Samango-Sprouse and A. Rogol, “XXY: the hidden disability and a prototype for an infantile presentation of developmental dyspraxia (IDD),” Infants and Young Children, vol. 15, no. 1, pp. 11–18, 2002. View at Google Scholar · View at Scopus
  8. J. L. Ross, D. P. Roeltgen, H. Kushner et al., “Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome,” Pediatrics, vol. 129, no. 4, pp. 769–778, 2012. View at Publisher · View at Google Scholar · View at Scopus
  9. N. Tartaglia, S. Davis, A. Hench et al., “A new look at XXYY syndrome: medical and psychological features,” American Journal of Medical Genetics, Part A, vol. 146, no. 12, pp. 1509–1522, 2008. View at Publisher · View at Google Scholar · View at Scopus
  10. L. Mutesa, M. Jamar, A. C. Hellin, G. Pierquin, and V. Bours, “A new 48,XXYY/47,XYY syndrome associated with multiple skeletal abnormalities, congenital heart disease and mental retardation,” Indian Journal of Human Genetics, vol. 18, no. 3, pp. 352–355, 2012. View at Publisher · View at Google Scholar · View at Scopus
  11. H. A. Delp, “Correlations between the Kent EGY and the Wechsler batteries,” Journal of Clinical Psychology, vol. 9, no. 1, pp. 73–75, 1953. View at Publisher · View at Google Scholar · View at Scopus
  12. N. Öner, Psychologic Tests Used in Turkey, Bogazici Universitesi Yayinlari, Istanbul, Turkey, 1997.
  13. S. R. Kay, A. Fiszbein, and L. A. Opler, “The positive and negative syndrome scale (PANSS) for schizophrenia,” Schizophrenia Bulletin, vol. 13, no. 2, pp. 261–276, 1987. View at Publisher · View at Google Scholar · View at Scopus
  14. S. Muldal, C. H. Ockey, M. Thompson, and L. L. White, “‘Double male’-a new chromosome constitution in the Klinefelter syndrome,” Acta Endocrinologica, vol. 39, pp. 183–203, 1962. View at Google Scholar · View at Scopus
  15. Genetic Home Reference, XXYY Syndrome, 2010.
  16. M. Borghgraef, J. P. Fryns, and H. Van Den Berghe, “The 48,XXYY syndrome. Follow-up data on clinical characteristics and psychological findings in 4 patients,” Genetic Counseling, vol. 2, no. 2, pp. 103–108, 1991. View at Google Scholar · View at Scopus
  17. J. Díaz-Atienza and M. P. Blánquez-Rodríguez, “Behavioral and neuropsychological phenotype of the 48,XXYY syndrome: a longitudinal study of a case,” Revista de Neurología, vol. 29, no. 10, pp. 926–929, 1999. View at Google Scholar · View at Scopus
  18. N. Borja-Santos, B. Trancas, P. S. Pinto et al., “48,XXYY in a general adult psychiatry department,” Psychiatry (Edgemont), vol. 7, no. 3, pp. 32–36, 2010. View at Google Scholar · View at Scopus
  19. J. Visootsak, N. Ayari, S. Howell, J. Lazarus, and N. Tartaglia, “Timing of diagnosis of 47,XXY and 48,XXYY: a survey of parent experiences,” American Journal of Medical Genetics, Part A, vol. 161, no. 2, pp. 268–272, 2013. View at Publisher · View at Google Scholar · View at Scopus
  20. B. Zantour, M. H. Sfar, S. Younes et al., “48XXYY syndrome in an adult with type 2 diabetes mellitus, unilateral renal aplasia, and pigmentary retinitis,” Case Reports in Medicine, vol. 2010, Article ID 612315, 5 pages, 2010. View at Publisher · View at Google Scholar