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CMT1B
Demyelinating
Autosomal Dominant
Associated Gene
MPZ
Chromosome
1q23.3
Zygosity
Heterozygous
CMT1B is caused by autosomal dominant mutations in the MPZ gene. CMT disease severity and age-at-onset varies greatly, from very severe CMT to very mild, and symptom onset anywhere between infancy and late adulthood. Age at onset does not determine disease severity.
Rev. Date
1/10/21
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