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- W2147766730 abstract "Germline testing for familial cases of myeloid leukemia in adults is becoming more common with the recognition of multiple genetic syndromes predisposing people to bone marrow disease. Currently, Clinical Laboratory Improvement Amendments approved testing exists for several myeloid leukemia predisposition syndromes: familial platelet disorder with propensity to acute myeloid leukemia (FPD/AML), caused by mutations in RUNX1; familial AML with mutated CEBPA; familial myelodysplastic syndrome and acute leukemia with mutated GATA2; and the inherited bone marrow failure syndromes, including dyskeratosis congenita, a disease of abnormal telomere maintenance. With the recognition of additional families with a genetic component to their leukemia, new predisposition alleles will likely be identified. We highlight how to recognize and manage these cases as well as outline the characteristics of the major known syndromes. We look forward to future research increasing our understanding of the scope of inherited myeloid leukemia syndromes." @default.
- W2147766730 created "2016-06-24" @default.
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- W2147766730 creator A5021387807 @default.
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- W2147766730 date "2013-05-03" @default.
- W2147766730 modified "2023-10-13" @default.
- W2147766730 title "Recognizing familial myeloid leukemia in adults" @default.
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- W2147766730 doi "https://doi.org/10.1177/2040620713487399" @default.
- W2147766730 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3734901" @default.
- W2147766730 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23926458" @default.
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