Title of article :
Trisomy 1q in a patient with severe aplastic anemia
Author/Authors :
Angelidis، نويسنده , , Prodromos and Kojouri، نويسنده , , Kiarash and Lee، نويسنده , , Jiyun and Kern، نويسنده , , William and Mulvihill، نويسنده , , John J. and Li، نويسنده , , Shibo، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
3
From page :
73
To page :
75
Abstract :
Aplastic anemia is a rare, serious disease characterized by hypocellular bone marrow and pancytopenia in the peripheral blood. Most cases are acquired, idiopathic, and without gross cytogenetic abnormalities. A few chromosome abnormalities have recurred among a small subset of patients, most commonly trisomy 8 and monosomy 7. Some of these chromosome abnormalities have prognostic and therapeutic significance, although for most the clinical relevance is not known. We present the case of a 40-year-old man with idiopathic severe aplastic anemia in bone marrow cells with trisomy of the whole long arm of chromosome 1 due to an unbalanced translocation between chromosomes 1 and 15 at breakpoints of q10 and 15q10. This clonal abnormality (which, to our knowledge, has not been previously reported in a patient with aplastic anemia) suggests that genes on 1q may be involved in marrow aplasia.
Journal title :
Cancer Genetics and Cytogenetics
Serial Year :
2006
Journal title :
Cancer Genetics and Cytogenetics
Record number :
1827824
Link To Document :
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