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Cancer Genet Cytogenet ; 169(1): 58-61, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16875938

ABSTRACT

We describe the rare finding of a 33-month-old child neonatally diagnosed with Down syndrome, who presented with pre-B acute lymphoblastic leukemia (ALL) with a pretreatment bone marrow karyotype in which a low hypodiploid cell line (38 chromosomes) was identified in 17/19 cells studied. The abnormal cell line retained the extra constitutional chromosome 21. Hypodiploidy (loss of one or more chromosomes) is seen in approximately 5% of all childhood pre-B ALL cases and in approximately 2.2% cases of individuals with a constitutional trisomy 21. Low hypodiploidy, associated with a high risk of relapse, is rare in pediatric ALL cases in the general population, and, to our knowledge, is previously unreported in patients with trisomy 21.


Subject(s)
Burkitt Lymphoma/genetics , Diploidy , Down Syndrome/genetics , Burkitt Lymphoma/complications , Child, Preschool , Down Syndrome/complications , Female , Humans , Karyotyping , Male
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