| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2816985 | Gene | 2013 | 4 Pages |
•The t(4;16)(q25;q23.1) rearrangement has never before been reported in AML•Classic and molecular cytogenetics allow novel rearrangements in AML to be defined•Deregulation of genes mapping next to the translocation breakpoints was detected
About 50% of acute myeloid leukemia (AML) patients show the occurrence of non-random chromosome rearrangements. Most of the recurrent karyotypic rearrangements in AML have been defined as distinct disease entities in the 2008 World Health Organization (WHO) classification. In this paper we report an AML case showing a novel t(4;16)(q25;q23.1) rearrangement causing the activation of epidermal growth factor (EGF) and elongation of long-chain fatty acids family member 6 (ELOVL6) genes, rather than the generation of a novel fusion gene.
