syndrome of Dejerine-Roussy - translation to arabic
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syndrome of Dejerine-Roussy - translation to arabic

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

syndrome of Dejerine-Roussy      
مُتَلاَزِمَةُ ديجيرين روسي
thalamic syndrome         
MEDICAL CONDITION
Dejerine-Roussy syndrome; Dejerine-Roussy disease; Thalamic pain syndrome; Thalamic pain; Dejerine-Roussy (Thalamic) Syndrome; Thalamic syndrome
‎ المُتَلاَزِمَةُ المِهادِيِّة‎
thalamic pain         
MEDICAL CONDITION
Dejerine-Roussy syndrome; Dejerine-Roussy disease; Thalamic pain syndrome; Thalamic pain; Dejerine-Roussy (Thalamic) Syndrome; Thalamic syndrome
‎ أَلَمٌ مِهادِيُّ المَنْشَأ‎

Definition

Reye's syndrome
['re?z, 'r??z]
¦ noun a life-threatening metabolic disorder in young children, of uncertain cause.
Origin
1960s: named after the Australian paediatrician Ralph D. K. Reye.

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.