Dejerine–Sottas disease

Also known as Charcot-Marie-Tooth type 3, Dejerine–Sottas syndrome, Dejerine–Sottas neuropathy, progressive hypertrophic interstitial polyneuropathy of childhood, onion bulb neuropathy, hereditary motor and sensory polyneuropathy type III

a rare hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting