Guest guest Posted August 11, 2005 Report Share Posted August 11, 2005 I am confused. My son was diagnosed with CMT, initially through an EMG, and then through DNA testing (CMT 1). My husband and I also were tested with an EMG, and were told, more or less definitively, that we do not have CMT, and that our son's condition is a 'one off' mutation. Is an EMG test definitive? We were told it was unnecessare for us (parents) to have any further testing. Regardless, I continue to wonder, because there are a few family members on both our sides that have experienced quite a bit of trouble with their feet and toes and lower limbs, in general. Because we have more than one child, I think it is important to seek the most reliable means of testing us, in order to feel more secure in the information I have that might apply to our other sons. Thank you! Debbie Quote Link to comment Share on other sites More sharing options...
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