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early onset/ Type 1C (DSS) /identical symptoms to 1A

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From http://en.wikipedia.org/wiki/Charcot-Marie-Tooth_disease

CMT type 1C - CMT1C - Sometimes called Dejerine-Sottas disease - Causes

severe demyelination, which can be detected by measuring nerve

conduction velocities. Autosomal dominant. Usually shows up in infancy.

LITAF Gene (16p13.1-p12.3) Average NCV: 26-42m/s. Identical symptoms to

CMT-1A.

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