Guest guest Posted February 9, 2002 Report Share Posted February 9, 2002 In a message dated 2/9/02 6:29:54 PM, rdick1@... writes: << With this in mind, why should anyone " not know " if they have CMT or not? >> I'm not Gretchen, but I'll throw in my two cents worth anyway. IF a person has one of the types that can be diagnosed using the DNA tests, that's easy. Many of the types can NOT be found that way. Only one of the many type 2s for example, are included in the tests. CMT Type 1-A , Type 1-B, CMTX (sex linked CMT), and HNPP can be tested for. (The test for 1-B has only been available for 2-3 years) There is also a new test for one of the mutations known in Type 2, but it is known that there are other mutations it will NOT detect. http://www.neuro.wustl.edu/neuromuscular/time/hmsn.html shows the currently known types. You will notice that Type 1 has a marked reduction in NCV's while Type 2 has only a slight slowing (possibly none at all)..Also note that many of the listed types are very rare and/or limited to those from certain ethnic backgrounds. Hope this helps clear it up. Kat Seattle USA Quote Link to comment Share on other sites More sharing options...
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