Charcot Marie Tooth disease 2M (CMT2M)

Evidence-based neurology checklist on charcot marie tooth disease 2m (cmt2m): Genetics This is caused by mutations in the DNM2 gene on chromosome 19p It is early onset age Clinical features Magnetic resonance imaging (MRI) muscle

Genetics

  • This is caused by mutations in the DNM2 gene on chromosome 19p
  • It is early onset age

Clinical features

Magnetic resonance imaging (MRI) muscle

References

  1. Fabrizi GM, Ferrarini M, Cavallaro T, et al. Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. Neurology 2007; 69:291-295.
  2. Gallardo E, Claeys KG, Nelis E, et al. Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation. J Neurol 2008; 255:986-992.

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