{Reference Type}: Journal Article
{Title}: Monosomy 7/del (7q) in inherited bone marrow failure syndromes: A systematic review.
{Author}: Pezeshki A;Podder S;Kamel R;Corey SJ;
{Journal}: Pediatr Blood Cancer
{Volume}: 64
{Issue}: 12
{Year}: Dec 2017
{Factor}: 3.838
{DOI}: 10.1002/pbc.26714
{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.