Keywords:
Down syndrome; GATA1; acute leukaemia; children; leukaemogenesis; myeloid leukaemia of Down syndrome; transient abnormal myelopoiesis
Abstract:
Children with Down syndrome (DS) are at increased risk of developing haematological malignancies, in particular acute megakaryoblastic leukaemia and acute lymphoblastic leukaemia. The microenvironment established by abnormal haematopoiesis driven by trisomy 21 is compounded by additional genetic and epigenetic changes that can drive leukaemogenesis in patients with DS.