(Q845618)

English

Dejerine–Sottas disease

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

  • 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
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