Philadelphia chromosome-negative chronic myelogenous leukemia in a child with t(8;9)(p11 or 12;q34)
- PMID: 6578689
Philadelphia chromosome-negative chronic myelogenous leukemia in a child with t(8;9)(p11 or 12;q34)
Abstract
Approximately 78% of chronic myelogenous leukemia patients have the standard Ph' chromosome-negative defect as their only chromosomal abnormality. CML has been extensively studied due to the availability of tumor tissue and the frequency and consistency with which such abnormalities are noted. There have been few cases reported, however, of Ph' chromosome-negative CML with an abnormality involving rearrangement and breaks at the 9q34 band. We report here a unique case of the fourth Ph'-negative patient who demonstrates this break.
Similar articles
-
[Abnormality of chromosome number 1 in 3 cases of acute transformation of chronic myeloid leukemia].Nouv Rev Fr Hematol (1978). 1984;26(5):303-8. Nouv Rev Fr Hematol (1978). 1984. PMID: 6594670 French.
-
Genomic diversity correlates with clinical variation in Ph'-negative chronic myeloid leukaemia.Nature. 1986 Mar 20-26;320(6059):281-3. doi: 10.1038/320281a0. Nature. 1986. PMID: 3007992
-
A complex translocation t(5;9;22) in Philadelphia cells involving the short arm of chromosome 5 in a case of chronic myelogenous leukemia.J Exp Clin Cancer Res. 2007 Sep;26(3):411-5. J Exp Clin Cancer Res. 2007. PMID: 17987804
-
Ph1-positive leukaemia, including chronic myelogenous leukaemia.Clin Haematol. 1980 Feb;9(1):55-86. Clin Haematol. 1980. PMID: 6245823 Review. No abstract available.
-
Chronic myelogenous leukemia and genetic events at 9q34.Hematol Oncol. 1983 Jul-Sep;1(3):269-74. doi: 10.1002/hon.2900010309. Hematol Oncol. 1983. PMID: 6376316 Review.
Cited by
-
Human tissue-type plasminogen activator gene located near chromosomal breakpoint in myeloproliferative disorder.Am J Hum Genet. 1986 Jul;39(1):79-87. Am J Hum Genet. 1986. PMID: 3092643 Free PMC article.
-
Reciprocal translocation between chromosomes 8 and 9 in atypical chronic myeloid leukaemia.J Med Genet. 1985 Oct;22(5):398-401. doi: 10.1136/jmg.22.5.398. J Med Genet. 1985. PMID: 3866076 Free PMC article.
-
Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13).Proc Natl Acad Sci U S A. 1998 May 12;95(10):5712-7. doi: 10.1073/pnas.95.10.5712. Proc Natl Acad Sci U S A. 1998. PMID: 9576949 Free PMC article.
-
[The 8p11 myeloproliferative syndrome].Med Klin (Munich). 1999 Apr 15;94(4):207-10. doi: 10.1007/BF03044856. Med Klin (Munich). 1999. PMID: 10373756 Review. German.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources