Guest guest Posted May 7, 2010 Report Share Posted May 7, 2010 Yes Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 7, 2010 Report Share Posted May 7, 2010 What type of cmt are we talking about? jenny In a message dated 5/7/2010 8:45:56 A.M. Pacific Daylight Time, cdwheels3@... writes: My sister and I were tested and found to have CMT. We know from neurological tests and clinic notes that we found of our now deceased father that he also had CMT. My brother does not appear to have any of the symptoms and possibly escaped the disease. Question: If there is a 50%/50% chance of inheriting the disease does that mean that the disease will not exist in the genes of my brother and his offspring? -wheels Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 7, 2010 Report Share Posted May 7, 2010 The neurologist has stated that our family has a unique CMT type close to HSN and has not suggested gene testing using the known commercially available tests. Gene testing is being planned for our next family reunion using a portable test kit and nerve conduction machine, blood would be draw, cheeks swabbed, etc. -wheels Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 7, 2010 Report Share Posted May 7, 2010 I hate to contradict Gretchen, so think of this as a little refinement of the answer ... If your brother was lucky enough to not inherit the gene that causes CMT (most usually autosomal dominant) then Gretchen is absolutely correct that his children will not inherit it (unless their mother has it -- not likely). HOWEVER, because CMT has variable penetrance, which means that some have a severe case, some have very mild cases and everything in between, your brother could still have the gene and be asymptomatic. In that case, he could pass it along. In my family one sister is significantly affected, I'm mildly affected and another sister seems asymptomatic. Her children are showing symptoms, though, and on closer examination, she is probably very mildly affected. Balance and hearing loss being her only definite symptoms. Holli > > Yes > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 Thanks Gretchen and Holli. We were found to be autosomal dominant. I am assuming that my brother was lucky. -wheels Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2010 Report Share Posted May 8, 2010 That is correct. My mother was the CMT carrier, My brother who is older than I does not have CMT, nor do his offsprings. My daughters do not seem to be affected and they are both in their 30's, which is older than I was when I knew I had inherited it. Margaret Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2010 Report Share Posted May 12, 2010 I do not have the original email about this thread but my paternal grandmother had CMT, they thought it was polio early on. She has two kids, my father and my aunt. Neither seem to have symptoms and are 70+ now. I have two brothers who do not have CMT and I show no signs either. None of my brothers kids or my aunts kids have CMT. My daughter does not have CMT but my 11 year old son definitely does. Weird stuff! Lori Quote Link to comment Share on other sites More sharing options...
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