Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 with Giant Axons

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 with Giant Axons, also known as autosomal dominant hereditary motor and sensory neuropathy type 2 with giant axons, is related to neuropathy, hereditary, with liability to pressure palsies and neuropathy, congenital hypomyelinating, 1, autosomal recessive. An important gene associated with Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 with Giant Axons is DCAF8 (DDB1 And CUL4 Associated Factor 8).