| Literature DB >> 28708320 |
Alex Pezeshki1, Shreya Podder2, Ralph Kamel2, Seth J Corey2.
Abstract
Inherited bone marrow failure syndromes (IBMFS) are rare cancer predisposition syndromes with an especially high risk of transformation to myelodysplastic syndrome (MDS) and/or acute myeloid leukemia (AML). We performed a retrospective systematic review of reported MDS/AML arising in the eight most common IBMFS to determine the frequency and outcome of chromosome 7 abnormalities. We identified 738 MDS/AML cases of 4,293 individuals. Monosomy 7 or del (7q) occurred in ∼17%. Greater understanding of the roles played by sequential acquisition of genetic and cytogenetic changes will provide insights into myeloid leukemogenesis and improve the surveillance and hopefully outcomes for individuals with IBMFS.Entities:
Keywords: acute myeloid leukemia; bone marrow failure syndromes; monosomy 7
Mesh:
Year: 2017 PMID: 28708320 PMCID: PMC5937691 DOI: 10.1002/pbc.26714
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167