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A rare t(X;21)(p11;q22) in childhood acute myeloid leukemia: A case report and literature review

2024-10-22

Abstract excerpt

The diagnosis and prognosis of acute myeloid leukemia (AML) are closely related to cytogenetic and molecular biological abnormalities in patients. t (X; 21) (p11; q22), as a novel rare recurrent genetic abnormality, has previously been reported in adult AML patients; it is predominant in males, is advanced in age, and is associated with shorter survival. Here, we report a female pediatric AML patient who carried t...

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Literature Corpus work
c64fd04d-b94a-59ff-97f7-0f0d0ff10388
DOI
10.22541/au.172959307.70484098/v1
Open publication

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