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der(3)t(3;5). Another recurring abnormality in myelodysplastic disorder.

作者信息

Lindgren V, Gibson L, Yang-Feng T L

机构信息

Department of Human Genetics, Yale University, New Haven, CT 06510.

出版信息

Cancer Genet Cytogenet. 1991 Jul 1;54(1):129-31. doi: 10.1016/0165-4608(91)90041-r.

DOI:10.1016/0165-4608(91)90041-r
PMID:2065307
Abstract

Monosomy for chromosome 5 or a portion of the long arm is a common finding in acute nonlymphocytic leukemia (ANLL) and myelodysplastic syndrome (MDS), especially when the disorder is therapy related [1,2]. If only a portion of chromosome 5 is missing, the loss is usually accomplished by interstitial deletion of various bands, most frequently q12-14 to q31-33 [3]. Occasionally monosomy for 5q is the result of a translocation between chromosome 5 and another chromosome, with the loss of the derivative chromosome that contains 5q. A previously described unbalanced translocation involves chromosome 7: [der(5)t(5;7)(q11.2;p11.2)] and appears to be a recurring abnormality in these disorders [4]. We report here one case of therapy related MDS, one case of MDS which may be therapy related, and two cases of MDS with another "variant" 5q - abnormality, namely a derivative chromosome 3 composed of most of the short arm of chromosome 5 and the long arm of chromosome 3: [der(3)t(3;5)(?p11;?p11)].

摘要

相似文献

1
der(3)t(3;5). Another recurring abnormality in myelodysplastic disorder.
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2
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