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Hi,
I won't pretend to know what 's wrong with you.
Originally when I first showed WCC abnormalities I had blood tests 2 a week for 6 weeks and was diagnosed with anaemia and cyclical neutropenia (non typical) my neutropenia also didn't follow the normal cyclical pattern but my doc decided to call it that anyway.
The neutrophils kept falling and gradually remained at levels below 0.5 so then the cyclical neutropenia tag was removed.
You can see from my signature what I turned out to have wrong with me.
Best of luck.
Chirley
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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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