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What (who) is syndrome of Dejerine-Roussy - definition

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

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.

https://en.wikipedia.org/wiki/Dejerine–Roussy_syndrome

Roussy–Lévy syndrome

HUMAN DISEASE

Roussy-Lévy disease; Roussy-Lévy syndrome; Roussy–Lévy hereditary areflexic dystasia; Roussy–Levy hereditary areflexic dystasia; Roussy–Levy syndrome; Roussy Levy hereditary areflexic dystasia; Roussy-Levy hereditary areflexic dystasia; Roussy-Lévy hereditary areflexic dystasia; Roussy-Levy syndrome

Roussy–Lévy syndrome, also known as Roussy–Lévy areflexic dystasia, is a rare disorder of humans that results in progressive muscle wasting. It is caused by mutation the s that code for proteins necessary for the functioning of the myelin sheath of the, affecting the conductance of nerve signals and resulting in loss of muscles' ability to move.

https://en.wikipedia.org/wiki/Roussy–Lévy_syndrome

Dejerine–Sottas disease

Dejerine–Sottas disease, also known as, 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 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.

https://en.wikipedia.org/wiki/Dejerine–Sottas_disease

Wikipedia

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.

https://en.wikipedia.org/wiki/Dejerine–Sottas disease