Guest guest Posted February 23, 2007 Report Share Posted February 23, 2007 Hello. I hope everyone is well today. My daughter is 7 (grade 1). Today we received genetic test results confirming she has CMT Type 1A. This is all very new to us. Although we have done a lot of reading on the web, we are still in the " collecting information " stage. One item that the Athena results said was that there was also an amino acit mutation of threonine to methionine in the PMP22 sequencing. Has anyone heard of this or its impact on CMT? Thanks - Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.