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Up to: Autosomal recessive intermediate Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease recessive intermediate A
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A is a subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by severe, early childhood-onset CMT neuropathy with prominent pes equinovarus deformity and impairment of hand muscles. Nerve conduction velocities usually range between 25-35 m/s and both axonal and demyelinating changes are observed on peripheral nerve pathology.
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Charcot-Marie-Tooth disease type 4A 2 trials