Prevalence and clinical correlates of JAK2 mutations in Down syndrome acute lymphoblastic leukaemia

Summary Recurrent, prognostically significant chromosomal abnormalities occur in approximately 75% of paediatric acute lymphoblastic leukaemia (ALL), but only infrequently in children with Down syndrome (DS) and ALL. Recently, novel somatic activating mutations in the gene Janus kinase 2 (JAK2) were...

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Veröffentlicht in:British journal of haematology 2009-03, Vol.144 (6), p.930-932
Hauptverfasser: Gaikwad, Amos, Rye, Cassia L., Devidas, Meenakshi, Heerema, Nyla A., Carroll, Andrew J., Izraeli, Shai, Plon, Sharon E., Basso, Giuseppe, Pession, Andrea, Rabin, Karen R.
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Sprache:eng
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Zusammenfassung:Summary Recurrent, prognostically significant chromosomal abnormalities occur in approximately 75% of paediatric acute lymphoblastic leukaemia (ALL), but only infrequently in children with Down syndrome (DS) and ALL. Recently, novel somatic activating mutations in the gene Janus kinase 2 (JAK2) were reported in 18% of DS ALL. Here we report identification and clinical correlates of JAK2 mutations in an independent cohort. JAK2 activating mutations occurred in 10/53 DS ALL cases (18·9%). Mutations were overrepresented in males (P 
ISSN:0007-1048
1365-2141
DOI:10.1111/j.1365-2141.2008.07552.x