| Literature DB >> 19477513 |
Huan-Ping Wang, Huan Xu, Zhi-Mei Chen, Xiang-Min Tong, Wen-Bin Qian, Jie Jin.
Abstract
We describe here a unique chromosomal abnormality found in a patient with M(3r) subtype of APL. Neither t(15;17) nor rearrangement of RARalpha was detected by routine R-banded chromosome as well as fluorescence in situ hybridization (FISH) analysis using PML/RARalpha dual-color dual-fusion translocation probe and RARalpha dual-color break apart rearrangement probe. Instead of the typical rearrangement between chromosomes 15 and 17, all cells analyzed had a translocation between X and 17 as the sole karyotypic anomaly. The translocation was conformed by whole chromosome painting (WCP) with painting probes of chromosomes X and 17. To our knowledge, this is the first documented APL with a novel translocation involving chromosomes X and 17 without RARalpha gene rearrangement. Copyright 2009. Published by Elsevier Ltd.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19477513 DOI: 10.1016/j.leukres.2009.04.034
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156