Dejerine-Sottas disease - definição. O que é Dejerine-Sottas disease. Significado, conceito
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O que (quem) é Dejerine-Sottas disease - definição

A RARE HEREDITARY NEUROLOGICAL DISORDER CHARACTERISED BY DAMAGE TO THE PERIPHERAL NERVES AND RESULTING PROGRESSIVE MUSCLE WASTING
Dejerine-Sottas syndrome; Déjerine-Sottas disease; DeJerine-Sottas Disease; Dejerine Sottas Syndrome; Dejerine sottas syndrome; Dejerine-Sottas neuropathy; Dejerine-Sottas; Dejerine Sottas syndrome; Dejerine-Sottas disease; Dejerine–Sottas syndrome; Dejerine–Sottas neuropathy

DejerineSottas disease         
DejerineSottas disease, also known as, DejerineSottas 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 a hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting. The condition is caused by mutations in a various genes and currently has no known cure.
Augusta Déjerine-Klumpke         
  • Jules and Augusta Dejerine
AMERICAN-BORN FRENCH MEDICAL DOCTOR (1859-1927)
Augusta Marie Klumpke; Augusta Dejerine-Klumpke; Augusta Marie Dejerine-Klumke; Augusta Klumpke
Augusta Déjerine-Klumpke (15 October 1859 – 5 November 1927) was an American-born French medical doctor known for her work in neuroanatomy. She was the first female intern to work in a hospital in Paris.
Dejerine–Roussy syndrome         
MEDICAL CONDITION
Dejerine-Roussy syndrome; Dejerine-Roussy disease; Thalamic pain syndrome; Thalamic pain; Dejerine-Roussy (Thalamic) Syndrome; Thalamic syndrome
Dejerine–Roussy syndrome or thalamic pain syndrome is a condition developed after a thalamic stroke, a stroke causing damage to the thalamus. Ischemic strokes and hemorrhagic strokes can cause lesioning in the thalamus.

Wikipédia

Dejerine–Sottas disease

Dejerine–Sottas disease, also known as, Dejerine–Sottas neuropathy, Dejerine–Sottas syndrome, progressive hypertrophic interstitial polyneuropathy of childhood, demyelinating polyneuropathy of childhood, and onion bulb neuropathy (and, hereditary motor and sensory polyneuropathy type III and Charcot–Marie–Tooth disease type 3), is a hereditary neurological disorder characterised by damage to the peripheral nerves, demyelination, and resulting progressive muscle wasting and somatosensory loss. The condition is caused by mutations in a various genes and currently has no known cure.

The disorder is named for Joseph Jules Dejerine and Jules Sottas, French neurologists who first described it.