Dear all.
A 65 year old patient, with acute myeloid leukemia, present the next karyotype (our interpretation):
- monosomy of chromosome 5
- trisomy of chromosome 9
- additional material in the p arm of chromosome 11
- chromosome 15 presents on p arm a segment of chromosome 17 band 17q24-17q21
Do you think our interpretation is correct?
What nomenclature should we use?
How do you describe a missing part on chromosome 17?