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Charcot-Marie-Tooth disease type 4E

rare

Charcot-Marie-Tooth disease type 4E (CMT4E) is a congenital, hypomyelinating subtype of Charcot-Marie-Tooth disease type 4 characterized by a Dejerine-Sottas syndrome-like phenotype (incl. hypotonia and/or delayed motor development in infancy), extremely slow nerve conduction velocities, potential respiratory dysfunction, cranial nerve involvement, and the typical CMT phenotype, i.e. distal muscle weakness and atrophy, sensory loss, and foot deformity.

Causal genes
EGR2
Also known as
autosomal recessive congenital hypomyelinating neuropathy · Charcot Marie Tooth disease type 4E · CHN · CHN1 · CMT 4E

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