Guest guest Posted May 17, 2005 Report Share Posted May 17, 2005 My husband finally had the Complete CMT genetic test from Athena. Medicare paid for it. One test, PMP22, was inconclusive, but when they repeated it, it was negative like all the others. What does this mean? Is there any next step? His neurologist thinks he has Type I. It was late onset, age 59, with little or no family history. (His mother complained of tingling in her fingers.) His son, 48, has hammer toes and feet just like his father's. His youngest son with pectus excavatum but normal looking feet wanted to know so he could get in vitro fertilization if he has the gene. Elinor Quote Link to comment Share on other sites More sharing options...
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