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3yr old CMT first thought to be type 2 now saying type 4

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I have a 3yr old daughter that has CMT we just went for our first MDA appt

yesterday and the Neurologist called me this morning to discuss her since she

was going to look over her info and the CMT info she had.

She has decided that with her symptoms/NCV/EMG/and the missense mutation in th

GDAP1 gene it is CMT 4 not CMT 2. So from what I have read about 4 is more

severe I can't find much about 4A but I did find something that said it

resembled 2K which was the first type that she fit. Without the genetic test

being positive I guess it's hard for them to say. We are being referred to

Genetics now.

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