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 HealthBoards Message Boards > Health Issues > Neuromuscular Diseases > CMT, Charcot Marie Tooth syndrome
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Old 11-11-2007, 12:10 PM   #1
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CMT, Charcot Marie Tooth syndrome
Anyone has CMT here? For mild CMT, will the nerve test show anything? Is only nerve biopsy or genetics can rule out CMT?

 
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Old 11-27-2007, 12:17 PM   #2
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Re: CMT, Charcot Marie Tooth syndrome
Yes a nerve test will tell if only mild. At least it did for me when I was 13. Pretty well suspected I did tho because my mother has CMT.

 
Old 12-04-2007, 04:19 PM   #3
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Re: CMT, Charcot Marie Tooth syndrome
i have had muscular atrophy since i was 23....am now 45...when they tested me they done both the biopsy and the nerve conduction test...I live in Australia so things might be dont different here..
Last edited by mermaidau5; 12-04-2007 at 04:20 PM.

 
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