Hi all you CMLers, I am anxious to find out if any of you have ever had monosomy 7, a missing chromosone 7. I have heard that this is rarely found in patients treated with Gleevec. Do you think it is the treatment, or that one chromosone mutation increases our likelihood of another? I am waiting on test results to confirm or deny monosomy 7 in my son. The waiting is the worst. I should find out late this week on the retest. Anyone out there encounter this (false Positive, or real positive result??)
Thanks, Sue Mom of Timmy, DX May 2007 600 mg gleevec, Cytogenetic remission Sept, 2008 --~--~---------~--~----~------------~-------~--~----~ [CMLHope] A support group of http://cmlhope.com ------------------------------------------------- You received this message because you are subscribed to the Google Groups "CMLHope" group. To post to this group, send email to [email protected] To unsubscribe from this group, send email to [EMAIL PROTECTED] For more options, visit this group at http://groups.google.com/group/CMLHope -~----------~----~----~----~------~----~------~--~---
