Guest guest Posted January 12, 2009 Report Share Posted January 12, 2009 My Dad has been recently diagnosed with CMT2 and gdadp1 was also mentioned. We have never had a case of CMT in the family that we know of. Supposedly, he could have messed him self genetically in another way during his life to cause this condition. Anyone else have this particular type, or feel that there condition is not hereditary? I looked up GDAP1, and it seems to be associated with CMT4A only. My Dad had no symptoms in his childhood, ran marathons etc. What other neuropathies are associated with GDAP1? I'm wondering if he has another condition, and want to cross reference any other condition with problems on the eighth chromosome, and other conditions that could cause a mutation in GDAP1. He doesn't seem to fit the profile. Any input would be appreciated. Quote Link to comment Share on other sites More sharing options...
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