Guest guest Posted September 18, 2008 Report Share Posted September 18, 2008 We have CMTX as well. The way I understand it, it passes through the X chromosome. If you are a girl, you get an X from each parent. If you are a guy you get an X from your mother and a Y from your father. Therefore, if you are a guy your daughter has a 50% chance of having the disease and most likely will be a carrier. Your sons will not get a defective gene from you. I am a female and passed it to my son. My mother has it, her father had it, his mother had it, etc. My mother's 2 brothers never had it. We have been able to trace it where the X passes along. My daughter is almost 20 and shows no signs yet so we don't know about her yet. I hope this answers your question. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2008 Report Share Posted September 22, 2008 My father was a carrier as well as had physical appearances of CMT. I also have the physical and conditions, but my brother does not have it, is only the two of us. I have three children 2 boys, one girl, and only my daughter has it. Can you maybe shine some light on that issue? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 CMT symptoms can appear so mild they go un-noticed. Members of the same family can all be affected differently and can even be diagnosed later in life. There are 5 types of CMT X. Has your family been through the DNA testing? Gretchen Quote Link to comment Share on other sites More sharing options...
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