Dejerine Sottas Syndrome
Dejerine–Sottas disease, also known as Dejerine–Sottas syndrome, Dejerine–Sottas neuropathy, progressive hypertrophic interstitial polyneuropathy of childhood and onion bulb neuropathy (and, hereditary motor and sensory polyneuropathy type III and Charcot–Marie–Tooth disease type 3), is an autosomal dominant or autosomal recessive neuropathy, which causes damage to the peripheral nerves.
Read more about Dejerine Sottas Syndrome: Eponym, Causes, Symptoms, Diagnosis
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