Literature DB >> 12505261

Identification of t(15;17) and a segmental duplication of chromosome 11q23 in a patient with acute myeloblastic leukemia M2.

Shibo Li1, Lijun Zhang, William F Kern, Dario Andrade, Jean E Forsberg, Francesca R Bates, John J Mulvihill.   

Abstract

A 32-year-old man was newly diagnosed with acute myelocytic leukemia, classified as acute myeloblastic leukemia with maturation (AML-M2) according to the French-American-British classification system. Conventional chromosome analysis before chemotherapy treatment revealed an abnormal karyotype: a possible segmental duplication of 11q23, plus a translocation between chromosomes 15 and 17 [t(15;17) (q22;q21.1)] in the majority of cells analyzed. Fluorescence in situ hybridization analysis using commercially available probes confirmed the cytogenetic findings. To our knowledge, this is the first report of a combination of t(15;17) and a segmental duplication of 11q23 in a patient with AML-M2.

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Year:  2002        PMID: 12505261     DOI: 10.1016/s0165-4608(02)00588-5

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  2 in total

1.  Quantifying the mechanisms for segmental duplications in mammalian genomes by statistical analysis and modeling.

Authors:  Yi Zhou; Bud Mishra
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-01       Impact factor: 11.205

2.  Trisomy 11 as an additional chromosome alteration in a child with acute promyelocytic leukemia with poor prognosis.

Authors:  Elenice Ferreira Bastos; Lidiane Alice Silva; Marcelo Coelho Ramos; Glicínia Pimenta; Paulo Ivo Cortez; Stella Beatriz Gonçalves de Lucena; Teresa de Souza Fernandez
Journal:  Case Rep Genet       Date:  2012-07-05
  2 in total

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