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Hi Kris, good news at last.
I have a question for you. I noticed in the signature that Ricki was found to have deletion13. Was this only found after the Vidaza treatment? Was it a partial deletion and was it p or q?
I'm only asking because I've just been found to have partial deletion 15q which wasn't there prior to Vidaza. My diagnosis has been changed from MDS to copper deficiency bone marrow failure so there is no disease process that could have caused this finding.
I'm not upset that I had Vidaza unnecessarily, Im just looking for answers.
Regards
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Copper deficiency bone marrow failure (MDS RAEB 1), neuromyelopathy.
FISH reported normal cytogenetics but gene testing showed
Xq 8.21 mutation
Xq19.36 mutation
Xq21.40. mutation
1p36. Mutation
15q11.2 deletion
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