Home > E. Pathology by systems > Nervous system > Peripheral nerves > CMT4A
CMT4A
Sunday 3 April 2005
Charcot-Marie-Tooth (CMT) type 4A is a severe autosomal recessive form of neuropathy associated with either demyelinating or axonal phenotypes.
Etiology
germline mutations in GDAP1 gene coding for ganglioside-induced differentiation-associated protein 1
