"This disease is named after French neurologist and pathologist Jean-Martin Charcot (1825-1893), often described as the "father of neurology", French neurologist Pierre Marie (1853-1940), and British neurologist Howard Henry Tooth (1856-1925) 6-8."
"autosomal recessive inheritance, due to mutation in SH3TC2 5"
"autosomal dominant inheritance, due to a mutation in MFN2 5"
"X-linked inheritance, due to a mutation in GJB1 (also known as connexin 32) 5"
Expected headings
"Demyelinating forms"
"Axonal forms"
"Intermediate forms"
"Peripheral nervous system"
"Central nervous system"
"characterised by infantile onset, resulting in severe peripheral demyelination with delayed motor skills; it is much more severe than CMT1A"
"Radiographic changes may be seen in the nervous system, or in secondary changes affecting the musculoskeletal system (e.g. pes cavus, scoliosis 16)."