Literature DB >> 7053756

Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia.

G W Dewald, R V Pierre, R L Phyliky.   

Abstract

Structural abnormalities of the X chromosome are rarely found in neoplastic disorders. We describe three patients with a history of idiopathic acquired sideroblastic anemia (IASA); each one had an abnormal clone of cells in the bone marrow, characterized by a structurally abnormal X chromosome. In two of these patients, the predominant karyotype was 47,X,2idic(X)(q13); in the other patient, it was 46,X,t(X;11)(q13;p15). Inasmuch as all three of these cases involved chromosome band Xq13, as did two previously published cases, we suggest that band Xq13 may be more prone to structural rearrangement than other X chromosome bands in hematologic disorders. The common Xq13 chromosome breakpoint and clinical presentation (IASA) among these three patients and the occurrence of an X-linked type of sideroblastic anemia may suggest that an association exists between X chromosome abnormalities and IASA. Perhaps alteration of a gene or chromosome structure in or near band Xq13 predisposes to development of IASA. The fact that two of these patients had preleukemia and the third had overt acute leukemia may imply that patients with IASA and X chromosome abnormalities have a poor prognosis. Cases of IASA without associated X chromosome abnormalities are known; thus, if an association between IASA and an abnormal X chromosome does exist, most likely it involves only some patients with IASA.

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Year:  1982        PMID: 7053756

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  6 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Triple X and erythroleukaemia.

Authors:  B Mulhern; S F Cahalane; J J Fennelly; E Lawlor; E Law
Journal:  Ir J Med Sci       Date:  1983-10       Impact factor: 1.568

4.  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

5.  Linkage analysis of a large pedigree with hereditary sideroblastic anaemia.

Authors:  J S Noble; G R Taylor; M S Losowsky; R Hall; G Turner; R F Mueller; A D Stewart
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

Review 6.  The molecular genetics of sideroblastic anemia.

Authors:  Sarah Ducamp; Mark D Fleming
Journal:  Blood       Date:  2018-11-06       Impact factor: 25.476

  6 in total

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