Guest guest Posted February 5, 2005 Report Share Posted February 5, 2005 I am 35 and was just officially diagnosed by a team of neurologists at UT Southwestern as having CMT1C. My genetic testing came back normal except for the f-Simple gene. That came back as a " variant of unknown significance " . Both of my parents were examined on the same day and neither of them showed any signs of CMT. The neurologists thought that one of them would for sure have signs of it and when both were normal they just told me that I must have a " spontaneous mutation " . Does anyone know what this means and whether this would be considered dominant or not. I just had a baby 10 months ago, and am obviously concerned that I have potentially passed this on to him. Also, I find little info on CMT1C on the net. Does anyone know where I might find more info on my particular type of CMT? Thank you - Amy Hodge Quote Link to comment Share on other sites More sharing options...
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