bn:03410583n
Noun Concept
Categories: Neurological disorders, Neurogenetic disorders, Rare diseases
EN
Dejerine–Sottas disease  Dejerine Sottas Syndrome  Dejerine-Sottas disease  Charcot-Marie-Tooth type 3  Dejerine-Sottas
EN
Dejerine–Sottas disease, also known as, Dejerine–Sottas syndrome, hereditary motor and sensory polyneuropathy type III, and Charcot–Marie–Tooth disease type 3, is a hereditary neurological disorder characterized by damage to the peripheral nerves, demyelination, and resulting progressive muscle wasting and somatosensory loss. Wikipedia
Definitions
Relations
Sources
EN
Dejerine–Sottas disease, also known as, Dejerine–Sottas syndrome, hereditary motor and sensory polyneuropathy type III, and Charcot–Marie–Tooth disease type 3, is a hereditary neurological disorder characterized by damage to the peripheral nerves, demyelination, and resulting progressive muscle wasting and somatosensory loss. Wikipedia
A rare hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting Wikidata