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Extreme hyperleukocytosis in a pediatric T-ALL patient with a rare translocation, t(7;19)(q35;p13), and submicroscopic deletions at 4q25, 7q33 and 10q23()

Although childhood T-cell acute lymphoblastic leukemia (T-ALL) is a high-risk disease the outcome can vary considerably. The varying outcomes suggest that unrecognized factors may contribute to disease progression. We report on a 2-year-old T-ALL patient presenting with a very short history of const...

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Detaylı Bibliyografya
Asıl Yazarlar: Veigaard, Christopher, Aggerholm, Anni, Hasle, Henrik, Kjeldsen, Eigil
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Elsevier 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3939383/
https://ncbi.nlm.nih.gov/pubmed/24596673
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.lrr.2013.09.004
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