Guest guest Posted November 18, 2009 Report Share Posted November 18, 2009 How do you classify cmt1A? does this mean we only have to take the ascorbic acid for 12 months? after 12 months what's next? thank you... Ascorbic Acid Well-Tolerated in Adults with CMT1A http://english. farsnews. net/newstext. php?nn=880820106 7 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 18, 2009 Report Share Posted November 18, 2009 Frederick, CMT 1A is one of the many genetic (DNA) classifications of CMT, and is the most common form, affecting 70-75% of all people with CMT. Ascorbic Acid for 1A is still in clinical trials - all over the world. The trials originated from the mouse study in 2004 which is in our Files section along with all the other trial studies thus far. Most studies up until now have concluded Ascorbic Acid doesn't change the phenotype of CMT 1A, however the trials have been short (12 months). The current USA trials are for 3 years, they began in 2007 (I think) so we'll have to wait for those. They are being conducted at three centers in the Eastern US. If CMT 1A is proved to be helped with Ascorbic Acid, researchers will have to work out recommended doses. Just another part of the process until we get theh full picture. If you search through our Archives from April 2004 onward, you'll find hundreds of posts from people who have self-experimented with different doses of Vitamin C (Ascorbic Acid), the amounts and the effects. CMT 1A is dominantly inherited and characterized by demylenation. More at http://neuromuscular.wustl.edu/time/hmsn.html#IA Gretchen 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.