Literature DB >> 10942809

A t(1;22)(p13;q13) in four children with acute megakaryoblastic leukemia (M7), two with Down syndrome.

R M Trejo1, R P Aguilera, S Nieto, S Kofman.   

Abstract

We report four children with acute megakaryoblastic leukemia (AML-M7) and t(1;22)(p13;q13), two of them with Down syndrome; their ages were 7 months, and 6, 7, and 10 years. These findings differ from those reported in children with M7 and t(1;22) at the age of presentation (exclusively under 1-year-old) and in the two cases associated with Down syndrome (t[1;22],+21c) that may be due to the high heterogeneity of the chromosomal changes in children with AML. We cannot disregard ethnic difference distribution of chromosomal changes and age of presentation in Mexican children with AML.

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Year:  2000        PMID: 10942809     DOI: 10.1016/s0165-4608(99)00251-4

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  1 in total

1.  Constitutional chromosomal abnormality identified in a sibling donor after bone marrow stem cell transplantation in a pediatric patient with acute megakaryoblastic leukemia.

Authors:  Bo-Young Seo; Hyun-Woo Choi; Min-Gu Kang; Duck Cho; Seung-Jung Kee; Soo-Hyun Kim; Jong-Hee Shin; Soon-Pal Suh; Dong-Wook Ryang; Myung-Geun Shin
Journal:  Ann Lab Med       Date:  2014-12-08       Impact factor: 3.464

  1 in total

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