A newborn with congenital mixed phenotype acute leukemia with complex translocation t(10;11)(p12;q23) with KMT2A/MLLT10 rearranged – a report of an extremely rare case

A newborn with congenital mixed phenotype acute leukemia with complex translocation t(10;11)(p12;q23) with KMT2A/MLLT10 rearranged – a report of an extremely rare case

Neonatal congenital leukemia (CL) constitutes less than 1% of all childhood leukemia cases and is diagnosed in 1 to 5 per million live births. In the neonatal period acute myeloid leukemia (AML) is described in 56-64% of cases, acute lymphoblastic leukemia (ALL) in 21-38% of cases and mixed-phenotyp...

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Bibliographic Details
Main Authors: Dawid Szpecht, Jolanta Skalska-Sadowska, Barbara Michniewicz, Janusz Gadzinowski, Ludmiła Machowska, Anna Pieczonka, Anna Przybyłowicz-Chalecka, Zuzanna Kanduła, Małgorzata Jarmuż-Szymczak, Krzysztof Lewandowski, Jacek Wachowiak
Format: Article
Language:English
Published: Termedia Publishing House 2018-10-01
Series:Central European Journal of Immunology
Subjects:
newborn
congenital leukemia
mixed phenotype acute leukemia
Online Access:https://www.termedia.pl/A-newborn-with-congenital-mixed-phenotype-acute-leukemia-with-complex-translocation-t-10-11-p12-q23-with-KMT2A-MLLT10-rearranged-a-report-of-an-extremely-rare-case,10,34298,1,1.html
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