Literature DB >> 3422047

Isodicentric X chromosomes involving the Xq13 breakpoint in myelodysplasia and acute nonlymphocytic leukemia.

W B Mackinnon1, P M Michael, L M Webber, O M Garson.   

Abstract

Many nonrandom chromosome abnormalities, usually autosomal in nature, have been found to be associated with specific types of acute nonlymphocytic leukemia (ANLL) and myelodysplastic syndromes (MDS). Specific abnormalities involving the sex chromosomes are rare. We have recently identified a structural abnormality of the X chromosome, for example, idic(X)(q13) in three patients: two with MDS progressing to ANLL and one with ANLL de novo. All three patients were elderly females with a very aggressive form of ANLL. Six other patients with a similar abnormality have been discovered in the literature; all having either MDS or ANLL and a short survival. It is suggested that the abnormality identifies a subset of MDS and ANLL occurring in elderly females.

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Year:  1988        PMID: 3422047     DOI: 10.1016/0165-4608(88)90091-x

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


  2 in total

1.  X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.

Authors:  W H Raskind; E Wijsman; R A Pagon; T C Cox; M J Bawden; B K May; T D Bird
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025

2.  Loss of ABCB7 gene: pathogenesis of mitochondrial iron accumulation in erythroblasts in refractory anemia with ringed sideroblast with isodicentric (X)(q13).

Authors:  Kazuya Sato; Yoshihiro Torimoto; Takaaki Hosoki; Katsuya Ikuta; Hiroyuki Takahashi; Masayo Yamamoto; Satoshi Ito; Naoka Okamura; Kazuhiko Ichiki; Hiroki Tanaka; Motohiro Shindo; Katsuyuki Hirai; Yusuke Mizukami; Takaaki Otake; Mikihiro Fujiya; Kastunori Sasaki; Yutaka Kohgo
Journal:  Int J Hematol       Date:  2011-03-08       Impact factor: 2.490

  2 in total

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