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Case Reports in Genetics
Volume 2012, Article ID 659016, 4 pages
http://dx.doi.org/10.1155/2012/659016
Case Report

Trisomy 11 as an Additional Chromosome Alteration in a Child with Acute Promyelocytic Leukemia with Poor Prognosis

1Faculty of Medical Sciences, State University of Rio de Janeiro, 20551-120 Rio de Janeiro, RJ, Brazil
2Bone Marrow Transplant Center, National Cancer Institute (INCA), 20551-120 Rio de Janeiro, RJ, Brazil
3Serviçio de Hematologia, Hospital Universitário Pedro Ernesto, Avenue 28 de Setembro no. 77, 3º andar, Vila Isabel, 20551-120 Rio de Janeiro, RJ, Brazil
4Hematology Service, HUCFF, UFRJ, 20551-120 Rio de Janeiro, RJ, Brazil
5Pronto Baby Children’s Hospital, 20551-120 Rio de Janeiro, RJ, Brazil

Received 14 February 2012; Accepted 11 June 2012

Academic Editors: P. D. Cotter, A. DeWan, B. Mittal, and A. M. Slavotinek

Copyright © 2012 Elenice Ferreira Bastos 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.

Citations to this Article [2 citations]

The following is the list of published articles that have cited the current article.

  • Yi He, Xudong Li, Dongning Wang, Erhong Zhang, Yuan Hu, Wenwen Wang, Renwei Huang, and Ruozhi Xiao, “Acute promyelocytic leukaemia with a PML-RARA insertional translocation and a chromosome 21 abnormality in XYY syndrome: Case report,” Journal Of International Medical Research, vol. 42, no. 6, pp. 1363–1373, 2014. View at Publisher · View at Google Scholar
  • Hongzai Guan, Jing Liu, Xiaofang Guo, Chunmei Wu, and Huawei Yu, “Microgranular variant of acute promyelocytic leukemia with der(17) ins(17;15): A case report and review of the literature,” Experimental And Therapeutic Medicine, vol. 10, no. 3, pp. 1009–1012, 2015. View at Publisher · View at Google Scholar