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t(1;2)(q12;q37)

Clinics and Pathology

Disease Acute leukemias
Note poorly known: only 3 cases to date
Phenotype / cell stem origin 1 case of M0 acute non lymphocytic leukemia (ANLL), 1 case of M4 ANLL, and 1 case of acute lymphoblastic leukemia (ALL)
Epidemiology a 76 yr old female patient, a 81 yr old male patient, and a 69 yr old male patient
Prognosis unknown

Cytogenetics

Cytogenetics Morphological The t(1;2) presented as a der(2)t(1;2) in at least 2 of the 3 cases, resulting in trisomy 1q. The t(1;2) was associated with a t(9;22) in 1 ANLL case and in the ALL case; +8 was found in 1 ANLL case and del( 7q) in the ALL case. The karyotypes were complex in 2 cases. The t(1;2) is likely to be a secondary anomaly.

External links

Other databaset(1;2)(q12;q37) Mitelman database (CGAP - NCBI)
Other databaset(1;2)(q12;q37) CancerChromosomes (NCBI)

To be noted

Additional cases are needed to delineate the epidemiology of this rare entity:
you are welcome to submit a paper to our new Case Report section.

Bibliography

Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders: rearrangements of DNA satellite II and new recurrent translocations.
Busson-Le Coniat M, Salomon-Nguyen F, Dastugue N, Maarek O, Lafage-Pochitaloff M, Mozziconacci MJ, Baranger L, Brizard F, Radford I, Jeanpierre M, Bernard OA, Berger R
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K. 1999 ; 13 (12) : 1975-1981.
PMID 10602418
 

Contributor(s)

Written02-2000Jean-Loup Huret

Citation

This paper should be referenced as such :
Huret JL . t(1;2)(q12;q37). Atlas Genet Cytogenet Oncol Haematol. February 2000 .
URL : http://AtlasGeneticsOncology.org/Genes/t0102q12q37ID1317.html

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indexed on : Sat Dec 6 18:02:02 2008


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