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Charcot-Marie-Tooth disease type 4B3

rare

Charcot-Marie-Tooth disease type 4B3 (CMT4B3) is a subtype of Charcot-Marie-Tooth type 4 characterized by a childhood onset of slowly progressing, demyelinating sensorimotor neuropathy, focally folded myelin sheaths in nerve biopsy, reduced nerve conduction velocities (less than 38 m/s), and the typical CMT phenotype (i.e. distal muscle weakness and atrophy, and sensory loss).

Causal genes
SBF1
Also known as
Charcot-Marie-Tooth disease type 4 caused by mutation in SBF1 · Charcot-Marie-Tooth disease with focally folded myelin · Charcot-Marie-Tooth disease, type 4B3 · CMT4B3 · SBF1 Charcot-Marie-Tooth disease type 4

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