
Factor H variants in paroxysmal nocturnal hemoglobinuria, the role of factor XII in SCD-related thrombosis, and clinical features of therapy-related NPM1-mutated AML
Blood Podcast
00:00
Overlapping Features of Therapy-Related and Dinovo NPM1 Mutated AML
NPM1 Mutated Acute Myload Leukemia, or AML, is a distinct subtype of leukemia with unique biological and pathological features. It accounts for approximately 30 to 35% of all adult AML cases. Therapy-related NPM1-mutated AML generally confers chemoresistance and a poor prognosis,. However, patients with therapy-related AML who also harbor the NPM1 mutation are rarely associated with 7Q deletion or deletion 7 chromosomal aberrations.
Transcript
Play full episode