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Case Reports in Genetics
Volume 2014, Article ID 517091, 4 pages
http://dx.doi.org/10.1155/2014/517091
Case Report

Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13

1Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain
2Centre of Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain
3Department of Pediatrics, University Hospital Virgen del Rocío, Avenida Manuel Siurot s/n, 41013 Seville, Spain
4Department of Neurophysiology, University Hospital Virgen del Rocío, Avenida Manuel Siurot s/n, 41013 Seville, Spain

Received 18 July 2014; Accepted 30 September 2014; Published 14 October 2014

Academic Editor: Jose Luis Royo

Copyright © 2014 Javier Sánchez 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.

How to Cite this Article

Javier Sánchez, Ana Peciña, Olga Alonso-Luengo, et al., “Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13,” Case Reports in Genetics, vol. 2014, Article ID 517091, 4 pages, 2014. https://doi.org/10.1155/2014/517091.