CMT1C

CMT1C

Demyelinating

Autosomal Dominant

Associated Gene

LITAF

Chromosome

16p13.13

Zygosity

Heterozygous

CMT1C is caused by autosomal dominant mutations in the LITAF gene. Disease presentation is typically similar to 1A, with symptom onset usually starting by the time the CMTer is in their 20s. A CMTer who has CMT1C will usually experience weakness in their feet and hands, and will experience sensory loss in the upper and lower limbs.

Rev. Date

1/10/21