| Literature DB >> 19641300 |
Hege K Vefring1, Franz X E Gruber, Line Wee, Randi Hovland, Henrik Hjorth-Hansen, Tobias Gedde Dahl, Peter Meyer.
Abstract
The BCR-ABL fusion gene represents the hallmark of chronic myelogenous leukemia (CML) and is derived from a translocation between chromosome 9 and 22. The majority of CML patients have a breakpoint in the major BCR region of the BCR gene giving rise to e13a2 or e14a2 BCR-ABL transcripts. Occasionally, other BCR breakpoints occur. The current report describes two e6a2 CML patients with imatinib treatment failure and unusual disease progression. One patient was Philadelphia chromosome positive and one was Philadelphia chromosome negative with an atypical BCR-ABL rearrangement, ins (22;9). 2009 S. Karger AG, BaselEntities:
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Year: 2009 PMID: 19641300 DOI: 10.1159/000230037
Source DB: PubMed Journal: Acta Haematol ISSN: 0001-5792 Impact factor: 2.195