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I don't know if this applies to CMT, but as far as I know, with genetics in

general, if the female is affected, there is a 50/50 chance of passing it on

with each pregnancy.

She has 2 X chromosomes, and only one would get passed on to each offspring. I

know that CMT is an X-linked disorder, so it can only be passed through the X.

An affected male would only pass it on to his daughters via the X, but not his

sons because of the Y. I know of other X-linked disorders where the mother

passes it on, but the unaffected X chromosome can take over, and no signs of the

disorder are apparent. Perhaps this could account for the parents who show no

signs, but the children do.

**** , not all CMT is X-linked. CMT Type 1 and CMT Type 2 and their

respective subtypes are NOT X-linked. Obviously X-linked CMT IS. Females with X

linked CMT CAN sometimes not show symptoms (meaning they are asytomatic). On the

other hand, I know CMT X females who show very serious symptoms. ~ Gretchen

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