If you follow me, you know I love tweeting about #HemePath and lately #AML subtypes🩸
So far, I’ve covered the subtypes of AML with recurrent genetic abnormalities (per WHO 2016) - see below if you’re interested! ⬇️
Looking forward to more HemePath #tweetorials in the future!
AML with mutated NPM1
AML with t(8;21)(q22;q22.1) RUNX1::RUNX1T1
AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22);CBFB-MYH11
APL with PML::RARA
AML with t(9;11)(p21.3;q23.3);MLLT3-KMT2A
AML with t(6;9)(p23;q34.1);DEK-NUP214
AML with inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOM
AML (megakaryoblastic) with t(1;22)(p13.3;q13.3);RBM15-MKL1
AML with biallelic mutations of CEBPA
Cases also archived on my website 🗂
✨ Always learning — welcome any feedback! And looking forward to more #HemePath soon! ✨
P.S. - if you liked this series, please consider voting for me & other lab professionals in this year’s #ASCP40UnderForty
ascp.org/content/get-in…
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