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Cancer Genet Cytogenet ; 169(1): 58-61, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16875938

RESUMO

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.


Assuntos
Linfoma de Burkitt/genética , Diploide , Síndrome de Down/genética , Linfoma de Burkitt/complicações , Pré-Escolar , Síndrome de Down/complicações , Feminino , Humanos , Cariotipagem , Masculino
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